Peptide-loaded dendritic-cell vaccination followed by treatment interruption for chronic HIV-1 infection: A phase 1 trial
Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adj...
Saved in:
Published in | Journal of Medical Virology Vol. 78; no. 6; pp. 711 - 718 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.06.2006
Wiley Wiley-Liss |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV‐1‐infected individuals. The safety and efficacy of DC‐based vaccine loaded with HIV‐1‐derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA‐A*2402 restriction were immunized to four HIV‐1‐infected individuals under HAART. In terms of safety, peptide‐loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN‐γ production in CD8+ lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non‐responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV‐1 infection. J. Med. Virol. 78:711–718, 2006. © 2006 Wiley‐Liss, Inc. |
---|---|
AbstractList | Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV-1-infected individuals. The safety and efficacy of DC-based vaccine loaded with HIV-1-derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA-A*2402 restriction were immunized to four HIV-1-infected individuals under HAART. In terms of safety, peptide-loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN-gamma production in CD8(+) lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non-responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV-1 infection.Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV-1-infected individuals. The safety and efficacy of DC-based vaccine loaded with HIV-1-derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA-A*2402 restriction were immunized to four HIV-1-infected individuals under HAART. In terms of safety, peptide-loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN-gamma production in CD8(+) lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non-responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV-1 infection. Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV-1-infected individuals. The safety and efficacy of DC-based vaccine loaded with HIV-1-derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA-A*2402 restriction were immunized to four HIV-1-infected individuals under HAART. In terms of safety, peptide-loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN-gamma production in CD8(+) lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non-responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV-1 infection. Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV-1-infected individuals. The safety and efficacy of DC-based vaccine loaded with HIV-1-derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA-A*2402 restriction were immunized to four HIV-1-infected individuals under HAART. In terms of safety, peptide-loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN- production in CD8+ lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non-responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV-1 infection. J. Med. Virol. 78:711-718, 2006. Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV‐1‐infected individuals. The safety and efficacy of DC‐based vaccine loaded with HIV‐1‐derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA‐A*2402 restriction were immunized to four HIV‐1‐infected individuals under HAART. In terms of safety, peptide‐loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN‐γ production in CD8+ lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non‐responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV‐1 infection. J. Med. Virol. 78:711–718, 2006. © 2006 Wiley‐Liss, Inc. Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART). Although which strategies for therapeutic vaccination are feasible remains controversial, application of dendritic cells (DCs) as a vaccine adjuvant represents a promising approach to improving deteriorated immune function in HIV‐1‐infected individuals. The safety and efficacy of DC‐based vaccine loaded with HIV‐1‐derived cytotoxic T lymphocytes (CTL) peptides were thus investigated in this study. Autologous DCs loaded with seven CTL peptides with HLA‐A*2402 restriction were immunized to four HIV‐1‐infected individuals under HAART. In terms of safety, peptide‐loaded DCs were well tolerated, and only mild local and general symptoms were observed during vaccine administration. ELISPOT assays to detect IFN‐γ production in CD8 + lymphocytes revealed a limited breadth of responses to immunized peptides in two of four participants, but no response in the remaining two participants. Differences in immunological response might be attributable to the fact that responders displayed higher nadir CD4 counts before starting HAART and were immunized with a larger number of DCs per reactive peptide than non‐responders. Discontinuation of HAART after vaccination failed to lower viral set points compared to those before starting HAART. This early outcome warrants further exploration to elucidate the therapeutic value of vaccination with DCs in HIV‐1 infection. J. Med. Virol. 78:711–718, 2006. © 2006 Wiley‐Liss, Inc. |
Author | Tomizawa, Mariko Iwamoto, Aikichi Kawana-Tachikawa, Ai Hosoya, Noriaki Nakamura, Tetsuya Odawara, Takashi Ide, Fuyuaki |
Author_xml | – sequence: 1 givenname: Fuyuaki surname: Ide fullname: Ide, Fuyuaki organization: Department of Infectious Diseases, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan – sequence: 2 givenname: Tetsuya surname: Nakamura fullname: Nakamura, Tetsuya email: tnakamur@ims.u-tokyo.ac.jp organization: Division of Infectious Diseases and Applied Immunology Research Hospital, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan – sequence: 3 givenname: Mariko surname: Tomizawa fullname: Tomizawa, Mariko organization: Department of Infectious Diseases, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan – sequence: 4 givenname: Ai surname: Kawana-Tachikawa fullname: Kawana-Tachikawa, Ai organization: Department of Infectious Diseases, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan – sequence: 5 givenname: Takashi surname: Odawara fullname: Odawara, Takashi organization: Division of Infectious Diseases and Applied Immunology Research Hospital, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan – sequence: 6 givenname: Noriaki surname: Hosoya fullname: Hosoya, Noriaki organization: Department of Infectious Diseases, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan – sequence: 7 givenname: Aikichi surname: Iwamoto fullname: Iwamoto, Aikichi organization: Department of Infectious Diseases, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan |
BackLink | https://cir.nii.ac.jp/crid/1871709542524873728$$DView record in CiNii http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17741889$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/16628588$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkV9PFDEUxRuDkQV98AuYeVATHwZuO9M_wxshsmBWNEbxsel07oTibGdtu8B-e7vsIomJ-tI2vb9zknvOHtnxo0dCXlI4oADs8Hp-c8BAUPaETCg0omxA0h0yAVqLUgjKd8lejNcAoBrGnpFdKgRTXKkJWX3GRXIdlsNoOuyKDn0XXHK2tDgMxY2x1nmT3OiLfhyG8TYz7apIAU2ao0-F8wlDWC62SCjsVRi9s8XZ-WVJ87hHu54dFcfF4spELGhWOzM8J097M0R8sb33ybfT919PzsrZp-n5yfGstJxKVnJmLMi2quoWu_xuW8D8z5uO5zkyocBywQxtjTJ11fcClbBC5TQotKCqffJ247sI488lxqTnLq6XMx7HZdRCNkA58P-CDDiHhlUZfLUFl-0cO70Ibm7CSj-kmoE3W8BEa4Y-GG9dfOSkrKlSTebebTgbxhgD9o8I6HWzOjer75vN7OEfrHXpvpgUjBv-pbh1A67-bq0_fLx8ULzeKLxz2X59UiWphIbXjLNayUqy9XrlBnMx4d1vYxN-5DAryfX3i6me1mo6-yKovqh-AfspzMw |
CODEN | JMVIDB |
CitedBy_id | crossref_primary_10_1016_j_vaccine_2011_02_095 crossref_primary_10_1111_j_1600_065X_2006_00440_x crossref_primary_10_1016_j_vaccine_2014_10_054 crossref_primary_10_1097_COH_0b013e3280119307 crossref_primary_10_3389_fimmu_2018_02993 crossref_primary_10_1002_jcb_30669 crossref_primary_10_1126_scitranslmed_3004682 crossref_primary_10_1016_j_clim_2011_10_010 crossref_primary_10_1016_S1473_3099_13_70343_8 crossref_primary_10_2217_imt_10_28 crossref_primary_10_1007_s10875_009_9313_9 crossref_primary_10_1111_j_1600_0463_2009_02544_x crossref_primary_10_3390_ijms17121985 crossref_primary_10_1080_21645515_2015_1012033 crossref_primary_10_3390_vaccines4010002 crossref_primary_10_1071_MA14028 crossref_primary_10_1016_j_jcyt_2012_11_012 crossref_primary_10_4236_wjv_2017_72002 crossref_primary_10_1002_eji_202149502 crossref_primary_10_1016_j_clim_2009_09_009 crossref_primary_10_1016_j_pharma_2014_11_003 crossref_primary_10_1093_infdis_jiq077 crossref_primary_10_1128_CVI_00221_07 crossref_primary_10_1155_2012_184979 crossref_primary_10_1097_QAD_0000000000002113 crossref_primary_10_1097_QAD_0b013e32825eabbc crossref_primary_10_1111_j_1365_2796_2008_02047_x crossref_primary_10_1016_j_humimm_2010_02_020 crossref_primary_10_1038_mt_2010_82 crossref_primary_10_1186_1742_4690_9_72 crossref_primary_10_1371_journal_pone_0074389 crossref_primary_10_1155_2024_6817965 crossref_primary_10_3181_0712_RM_349 crossref_primary_10_1155_2020_9470102 crossref_primary_10_2217_imt_09_68 crossref_primary_10_4161_hv_19555 crossref_primary_10_1016_j_vaccine_2009_05_028 crossref_primary_10_1016_j_vaccine_2012_03_075 crossref_primary_10_2217_imt_10_91 crossref_primary_10_1097_QAD_0b013e328344cea5 crossref_primary_10_7448_IAS_18_1_20497 crossref_primary_10_1038_s41577_021_00649_1 crossref_primary_10_1111_imr_12082 crossref_primary_10_1016_j_semcdb_2018_02_015 crossref_primary_10_1111_imr_12083 crossref_primary_10_1371_journal_pone_0022939 crossref_primary_10_1586_erv_10_68 crossref_primary_10_1007_s11904_012_0113_0 crossref_primary_10_4161_hv_25876 crossref_primary_10_1016_j_trivac_2013_12_001 crossref_primary_10_1016_j_vaccine_2011_07_043 crossref_primary_10_1016_j_vetimm_2009_10_012 crossref_primary_10_1186_s12981_021_00426_z crossref_primary_10_1016_j_micinf_2007_01_021 crossref_primary_10_1080_14760584_2017_1322513 crossref_primary_10_1016_j_vaccine_2011_05_096 crossref_primary_10_2217_imt_2017_0165 crossref_primary_10_1007_s00262_008_0493_6 crossref_primary_10_4049_jimmunol_181_4_2356 crossref_primary_10_1586_14760584_7_1_131 |
Cites_doi | 10.1073/pnas.202372199 10.1038/71577 10.1177/135965350501000212 10.1182/blood.V98.6.1872 10.1016/0198-8859(86)90006-6 10.1097/00002030-200309260-00002 10.1038/nri1592 10.1038/nm880 10.1128/jvi.68.9.6103-6110.1994 10.1371/journal.pmed.0010036 10.1158/0008-5472.CAN-03-3505 10.1128/JVI.68.7.4650-4655.1994 10.4049/jimmunol.170.8.4260 10.1097/00002030-200211220-00018 10.1001/archinte.163.10.1220 10.1046/j.1468-1293.2003.00148.x 10.1128/JVI.79.13.8024-8031.2005 10.1097/00002030-200501030-00004 10.1038/nm1147 10.1128/JVI.73.2.1708-1714.1999 10.4049/jimmunol.159.12.6242 10.1097/00002030-199815000-00020 10.1146/annurev.immunol.18.1.767 10.1128/JVI.78.16.8437-8445.2004 10.1086/379215 10.1016/j.vaccine.2005.04.013 10.1086/429340 10.1038/35073658 10.4049/jimmunol.158.7.3325 10.1097/00002030-200104130-00006 10.1016/j.vaccine.2003.09.049 10.1086/432002 10.1097/00002030-200305020-00021 |
ContentType | Journal Article |
Copyright | Copyright © 2006 Wiley‐Liss, Inc. 2006 INIST-CNRS |
Copyright_xml | – notice: Copyright © 2006 Wiley‐Liss, Inc. – notice: 2006 INIST-CNRS |
DBID | BSCLL RYH AAYXX CITATION IQODW CGR CUY CVF ECM EIF NPM 7T5 7U9 H94 7X8 |
DOI | 10.1002/jmv.20612 |
DatabaseName | Istex CiNii Complete CrossRef Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Immunology Abstracts Virology and AIDS Abstracts AIDS and Cancer Research Abstracts MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) AIDS and Cancer Research Abstracts Immunology Abstracts Virology and AIDS Abstracts MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic MEDLINE AIDS and Cancer Research Abstracts CrossRef |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1096-9071 |
EndPage | 718 |
ExternalDocumentID | 16628588 17741889 10_1002_jmv_20612 JMV20612 ark_67375_WNG_G48GLR61_N |
Genre | article Research Support, Non-U.S. Gov't Journal Article Clinical Trial, Phase I |
GrantInformation_xml | – fundername: Ministry of Health, Labor and Welfare of Japan – fundername: The Special Coordination Funds for Promoting Science and Technology of MEXT |
GroupedDBID | --- .3N .55 .GA .GJ .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 31~ 33P 3O- 3SF 3WU 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52R 52S 52T 52U 52V 52W 52X 53G 5GY 5RE 5VS 66C 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A01 A03 AAESR AAEVG AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABEML ABIJN ABJNI ABOCM ABPVW ABQWH ABXGK ACAHQ ACBWZ ACCFJ ACCZN ACGFS ACGOF ACMXC ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFFNX AFFPM AFGKR AFPWT AFRAH AFZJQ AHBTC AHMBA AI. AIACR AITYG AIURR AIWBW AJBDE ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ASPBG ATUGU AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BMXJE BROTX BRXPI BSCLL BY8 C45 CS3 D-6 D-7 D-E D-F DCZOG DPXWK DR2 DRFUL DRMAN DRSTM DU5 EBD EBS ECGQY EJD ELTNK EMOBN F00 F01 F04 F5P FEDTE FUBAC G-S G.N GNP GODZA H.X HBH HF~ HGLYW HHY HHZ HVGLF HZ~ IX1 J0M JPC KBYEO KQQ L7B LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES M65 MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG OVD P2P P2W P2X P2Z P4B P4D PALCI PQQKQ Q.N Q11 QB0 QRW R.K RGB RIWAO RJQFR ROL RWI RX1 RYL SAMSI SUPJJ SV3 TEORI TUS UB1 V2E VH1 W8V W99 WBKPD WHG WIB WIH WIJ WIK WJL WNSPC WOHZO WQJ WRC WUP WXI WXSBR WYISQ X7M XG1 XPP XV2 ZGI ZXP ZZTAW ~IA ~KM ~WT AAHQN AAIPD AAMNL AANHP AAYCA ACRPL ACYXJ ADNMO AEYWJ AFWVQ AGQPQ AGYGG ALVPJ RYH AAYXX AGHNM CITATION AAMMB AEFGJ AGXDD AIDQK AIDYY IQODW CGR CUY CVF ECM EIF NPM 7T5 7U9 H94 7X8 |
ID | FETCH-LOGICAL-c5172-52ac07b334bed2acbb0e17259d5517e2680c562a1ba8a43ff6e86c6861210b083 |
IEDL.DBID | DR2 |
ISSN | 0146-6615 |
IngestDate | Fri Jul 11 03:19:20 EDT 2025 Fri Jul 11 16:43:03 EDT 2025 Wed Feb 19 01:52:48 EST 2025 Mon Jul 21 09:13:54 EDT 2025 Thu Apr 24 23:07:32 EDT 2025 Tue Jul 01 01:33:15 EDT 2025 Wed Jan 22 16:27:24 EST 2025 Thu Jun 26 22:39:28 EDT 2025 Wed Oct 30 09:54:44 EDT 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 6 |
Keywords | HIV-1 Immunopathology Dendritic cell Peptides HIV-1 virus Vaccination Retroviridae AIDS Vaccine Immune deficiency Lentivirus Infection Virus treatment interruption Chronic Treatment Viral disease Antiviral Human immunodeficiency virus HAART |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor CC BY 4.0 |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c5172-52ac07b334bed2acbb0e17259d5517e2680c562a1ba8a43ff6e86c6861210b083 |
Notes | Ministry of Health, Labor and Welfare of Japan The Special Coordination Funds for Promoting Science and Technology of MEXT istex:1CE295369BBA33F11CB19A57790136C65869BB36 ark:/67375/WNG-G48GLR61-N ArticleID:JMV20612 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
PMID | 16628588 |
PQID | 20550923 |
PQPubID | 23462 |
PageCount | 8 |
ParticipantIDs | proquest_miscellaneous_67901505 proquest_miscellaneous_20550923 pubmed_primary_16628588 pascalfrancis_primary_17741889 crossref_primary_10_1002_jmv_20612 crossref_citationtrail_10_1002_jmv_20612 wiley_primary_10_1002_jmv_20612_JMV20612 nii_cinii_1871709542524873728 istex_primary_ark_67375_WNG_G48GLR61_N |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | June 2006 |
PublicationDateYYYYMMDD | 2006-06-01 |
PublicationDate_xml | – month: 06 year: 2006 text: June 2006 |
PublicationDecade | 2000 |
PublicationPlace | Hoboken |
PublicationPlace_xml | – name: Hoboken – name: New York, NY – name: United States |
PublicationTitle | Journal of Medical Virology |
PublicationTitleAlternate | J. Med. Virol |
PublicationYear | 2006 |
Publisher | Wiley Subscription Services, Inc., A Wiley Company Wiley Wiley-Liss |
Publisher_xml | – name: Wiley Subscription Services, Inc., A Wiley Company – name: Wiley – name: Wiley-Liss |
References | Banchereau J, Briere F, Caux C, Davoust J, Lebecque S, Liu YJ, Pulendran B, Palucka K. 2000. Immunobiology of dendritic cells. Annu Rev Immunol 18: 767-811. Lee Sp, Tierney RJ, Thomas WA, Brooks JM, Rickinson AB. 1997. Conserved CTL epitopes within EBV latent membrane protein 2. J Immunol 158: 3325-3334. Kinloch-de Loes S, Hoen B, Smith DE, Autran B, Lampe FC, Phillips AN, Goh LE, Andersson J, Tsoukas C, Sonnerborg A, Tambussi G, Girard PM, Bloch M, Battegay M, Carter N, El Habib R, Theofan G, Cooper DA, Perrin L, QUEST Study Group. 2005. Impact of therapeutic immunization on HIV-1 viremia after discontinuation of antiretroviral therapy initiated during acute infection. J Infect Dis 192: 607-617. Kuzushima K, Hayashi N, Kimura H, Tsurumi T. 2001. Efficient identification of HLA-A*2402-restricted cytomegalovirus-specific CD8+ T-cell epitopes by a computer algorithm and an enzyme-linked immunospot assay. Blood 98: 1872-1881. Borrow P, Lewicki H, Hahn BH, Shaw GM, Oldstone MB. 1994. Virus-specific CD8 cytotoxic T-lymphocyte activity associated with control of viremia in primary human immunodeficiency virus type 1 infection. J Virol 68: 6103-6110. Koup RA, Safrit JT, Cao Y, Andrews CA, McLeod G, Borkowsky W, Farthing C, Ho DD. 1994. Temporal association of cellular immune responses with the initial control of viremia in primary human immunodeficiency virus type 1 syndrome. J Virol 68: 4650-4655. Lu W, Arraes LC, Ferreira WT, Andrieu JM. 2004. Therapeutic dendritic-cell vaccine for chronic HIV-1 infection. Nat Med 10: 1359-1365. Bostrom AC, Hejdeman B, Matsuda R, Fredriksson M, Fredriksson EL, Bratt G, Sandstrom E, Wahren B. 2004. Long-term persistence of vaccination and HAART to human immunodeficiency virus (HIV). Vaccine 22: 1683-1691. Metzner KJ, Bonhoeffer S, Fischer M, Karanicolas R, Allers K, Joos B, Weber R, Hirschel B, Kostrikis LG, Gunthard HF, The Swiss HIV Cohort Study. 2003. Emergence of minor populations of human immunodeficiency virus type 1 carrying the M184V and L90M mutations in subjects undergoing structured treatment interruptions. J Infect Dis 188: 1433-1443. Ramratnam B, Mittler JE, Zhang L, Boden D, Hurley A, Fang F, Macken CA, Perelson AS, Markowitz M, Ho DD. 2000. The decay of the latent reservoir of replication-competent HIV-1 is inversely correlated with the extent of residual viral replication during prolonged anti-retroviral therapy. Nat Med 6: 82-85. Dorrell L, Dong T, Ogg GS, Lister S, McAdam S, Rostron T, Conlon C, McMichael AJ, Rowland-Jones SL. 1999. Distinct recognition of non-clade B human immunodeficiency virus type 1 epitopes by cytotoxic T lymphocytes generated from donors infected in Africa. J Virol 73: 1708-1714. Furutsuki T, Hosoya N, Kawana-Tachikawa A, Tomizawa M, Odawara T, Goto M, Kitamura Y, Nakamura T, Kelleher AD, Cooper DA, Iwamoto A. 2004. Frequent transmission of cytotoxic-T-lymphocyte escape mutants of human immunodeficiency virus type 1 in the highly HLA-A24-positive Japanese population. J Virol 78: 8437-8445. Lisziewicz J, Trocio J, Xu J, Whitman L, Ryder A, Bakare N, Lewis MG, Wagner W, Pistorio A, Arya S, Lori F. 2005. Control of viral rebound through therapeutic immunization with DermaVir. AIDS 19: 35-43. Oxenius A, Price DA, Gunthard HF, Dawson SJ, Fagard C, Perrin L, Fischer M, Weber R, Plana M, Garcia F, Hirschel B, McLean A, Phillips RE. 2002. Stimulation of HIV-specific cellular immunity by structured treatment interruption fails to enhance viral control in chronic HIV infection. Proc Natl Acad Sci USA 99: 13747-13752. Ikeda-Moore Y, Tomiyama H, Miwa K, Oka S, Iwamoto A, Kaneko Y, Takiguchi M. 1997. Identification and characterization of multiple HLA-A24-restricted HIV-1 CTL epitopes: Strong epitopes are derived from V regions of HIV-1. J Immunol 159: 6242-6252. Tanaka H, Akaza T, Juji T. 1996. Report of the Japanese Central Bone Marrow Data Center. Clin Transpl 139-144. Kaufmann DE, Lichterfeld M, Altfeld M, Addo MM, Johnston MN, Lee PK, Wagner BS, Kalife ET, Strick D, Rosenberg ES, Walker BD. 2004. Limited durability of viral control following treated acute HIV infection. PLoS Med 1: e36. Watanabe N, Tomizawa M, Tachikawa-Kawana A, Goto M, Ajisawa A, Nakamura T, Iwamoto A. 2001. Quantitative and qualitative abnormalities in HIV-1-specific T cells. AIDS 15: 711-715. Kawamura T, Gatanaga H, Borris DL, Connors M, Mitsuya H, Blauvelt A. 2003. Decreased stimulation of CD4+ T cell proliferation and IL-2 production by highly enriched populations of HIV-infected dendritic cells. J Immunol 170: 4260-4266. Tremblay CL, Hicks JL, Sutton L, Giguel F, Flynn T, Johnston M, Sax PE, Walker BD, Hirsch MS, Rosenberg ES, D'Aquila RT. 2003. Antiretroviral resistance associated with supervised treatment interruptions in treated acute HIV infection. AIDS 17: 1086-1089. Garcia F, Lejeune M, Climent N, Gil C, Alcami J, Morente V, Alos L, Ruiz A, Setoain J, Fumero E, Castro P, Lopez A, Cruceta A, Piera C, Florence E, Pereira A, Libois A, Gonzalez N, Guila M, Caballero M, Lomena F, Joseph J, Miro JM, Pumarola T, Plana M, Gatell JM, Gallart T. 2005. Therapeutic immunization with dendritic cells loaded with heat-inactivated autologous HIV-1 in patients with chronic HIV-1 infection. J Infect Dis 191: 1680-1685. Banchereau J, Palucka AK. 2005. Dendritic cells as therapeutic vaccines against cancer. Nat Rev Immunol 5: 296-306. Schweighardt B, Ortiz GM, Grant RM, Wellons M, Miralles GD, Kostrikis LG, Bartlett JA, Nixon DF. 2002. Emergence of drug-resistant HIV-1 variants in patients undergoing structured treatment interruptions. AIDS 16: 2342-2344. McMichael AJ, Rowland-Jones SL. 2001. Cellular immune responses to HIV. Nature 410: 980-987. Fagard C, Oxenius A, Gunthard H, Garcia F, Le Braz M, Mestre G, Battegay M, Furrer H, Vernazza P, Bernasconi E, Telenti A, Weber R, Leduc D, Yerly S, Price D, Dawson SJ, Klimkait T, Perneger TV, McLean A, Clotet B, Gatell JM, Perrin L, Plana M, Phillips R, Hirschel B, Swiss HIV Cohort Study. 2003. A prospective trial of structured treatment interruptions in human immunodeficiency virus infection. Arch Intern Med 163: 1220-1226. Siliciano JD, Kajdas J, Finzi D, Quinn TC, Chadwick K, Margolick JB, Kovacs C, Gange SJ, Siliciano RF. 2003. Long-term follow-up studies confirm the stability of the latent reservoir for HIV-1 in resting CD4+ T cells. Nat Med 9: 727-728. Tubiana R, Carcelain G, Vray M, Gourlain K, Dalban C, Chermak A, Rabian C, Vittecoq D, Simon A, Bouvet E, El Habib R, Costagliola D, Calvez V, Autran B, Katlama C, the Vacciter Study group. 2005. Therapeutic immunization with a human immunodeficiency virus (HIV) type 1-recombinant canarypox vaccine in chronically HIV-infected patients: The Vacciter Study (ANRS 094). Vaccine 23: 4292-4301. Wu L, Kong WP, Nabel GJ. 2005. Enhanced breadth of CD4 T-cell immunity by DNA prime and adenovirus boost immunization to human immunodeficiency virus Env and Gag immunogens. J Virol 79: 8024-8031. Yu JS, Liu G, Ying H, Yong WH, Black KL, Wheeler CJ. 2004. Vaccination with tumor lysate-pulsed dendritic cells elicits antigen-specific, cytotoxic T-cells in patients with malignant glioma. Cancer Res 64: 4973-4979. Harrer E, Bauerle M, Ferstl B, Chaplin P, Petzold B, Mateo L, Handley A, Tzatzaris M, Vollmar J, Bergmann S, Rittmaier M, Eismann K, Muller S, Kalden JR, Spriewald B, Willbold D, Harrer T. 2005. Therapeutic vaccination of HIV-1-infected patients on HAART with a recombinant HIV-1 nef-expressing MVA: Safety, immunogenicity and influence on viral load during treatment interruption. Antivir Ther 10: 285-300. Ikeda-Moore Y, Tomiyama H, Ibe M, Oka S, Miwa K, Kaneko Y, Takiguchi M. 1998. Identification of a novel HLA-A24-restricted cytotoxic T-lymphocyte epitope derived from HIV-1 Gag protein. AIDS 12: 2073-2074. Lange CG, Lederman MM, Medvik K, Asaad R, Wild M, Kalayjian R, Valdez H. 2003. Nadir CD4+ T-cell count and numbers of CD28+ CD4+ T-cells predict functional responses to immunizations in chronic HIV-1 infection. AIDS 17: 2015-2023. Foung SK, Taidi B, Ness D, Grumet FC. 1986. A monoclonal antibody against HLA-A11 and A24. Hum Immunol 15: 316-319. Hejdeman B, Leandersson AC, Fredriksson EL, Sandstrom E, Wahren B, Bratt G. 2003. Better preserved immune responses after immunization with rgp 160 in HIV-1 infected patients treated with highly active antiretroviral therapy than in untreated patients with similar CD4 levels during at 2 years' follow-up. HIV Med 4: 101-110. 2002; 16 2004; 22 2005; 191 1997; 158 1997; 159 2005; 192 2004; 64 2000; 6 1986; 15 2002; 99 1996 1994; 68 2003; 170 2003; 17 2004; 1 2005; 23 2004; 10 2001; 410 2000; 18 2005; 19 2004; 78 2003; 9 2005; 5 2003; 4 2005; 10 2001; 15 1999; 73 1998; 12 2003; 188 2005; 79 2003; 163 2001; 98 Lee Sp (e_1_2_1_21_1) 1997; 158 Borrow P (e_1_2_1_4_1) 1994; 68 Ikeda‐Moore Y (e_1_2_1_13_1) 1997; 159 Harrer E (e_1_2_1_11_1) 2005; 10 e_1_2_1_20_1 e_1_2_1_23_1 e_1_2_1_24_1 e_1_2_1_22_1 e_1_2_1_27_1 e_1_2_1_28_1 e_1_2_1_25_1 e_1_2_1_26_1 e_1_2_1_29_1 Dorrell L (e_1_2_1_6_1) 1999; 73 e_1_2_1_7_1 e_1_2_1_31_1 e_1_2_1_8_1 e_1_2_1_5_1 e_1_2_1_3_1 e_1_2_1_12_1 e_1_2_1_35_1 e_1_2_1_34_1 e_1_2_1_10_1 e_1_2_1_33_1 e_1_2_1_2_1 e_1_2_1_32_1 e_1_2_1_16_1 Tanaka H (e_1_2_1_30_1) 1996 e_1_2_1_17_1 e_1_2_1_14_1 e_1_2_1_15_1 e_1_2_1_9_1 e_1_2_1_18_1 e_1_2_1_19_1 |
References_xml | – reference: Yu JS, Liu G, Ying H, Yong WH, Black KL, Wheeler CJ. 2004. Vaccination with tumor lysate-pulsed dendritic cells elicits antigen-specific, cytotoxic T-cells in patients with malignant glioma. Cancer Res 64: 4973-4979. – reference: Kinloch-de Loes S, Hoen B, Smith DE, Autran B, Lampe FC, Phillips AN, Goh LE, Andersson J, Tsoukas C, Sonnerborg A, Tambussi G, Girard PM, Bloch M, Battegay M, Carter N, El Habib R, Theofan G, Cooper DA, Perrin L, QUEST Study Group. 2005. Impact of therapeutic immunization on HIV-1 viremia after discontinuation of antiretroviral therapy initiated during acute infection. J Infect Dis 192: 607-617. – reference: Wu L, Kong WP, Nabel GJ. 2005. Enhanced breadth of CD4 T-cell immunity by DNA prime and adenovirus boost immunization to human immunodeficiency virus Env and Gag immunogens. J Virol 79: 8024-8031. – reference: Tanaka H, Akaza T, Juji T. 1996. Report of the Japanese Central Bone Marrow Data Center. Clin Transpl 139-144. – reference: Hejdeman B, Leandersson AC, Fredriksson EL, Sandstrom E, Wahren B, Bratt G. 2003. Better preserved immune responses after immunization with rgp 160 in HIV-1 infected patients treated with highly active antiretroviral therapy than in untreated patients with similar CD4 levels during at 2 years' follow-up. HIV Med 4: 101-110. – reference: Kawamura T, Gatanaga H, Borris DL, Connors M, Mitsuya H, Blauvelt A. 2003. Decreased stimulation of CD4+ T cell proliferation and IL-2 production by highly enriched populations of HIV-infected dendritic cells. J Immunol 170: 4260-4266. – reference: Ikeda-Moore Y, Tomiyama H, Ibe M, Oka S, Miwa K, Kaneko Y, Takiguchi M. 1998. Identification of a novel HLA-A24-restricted cytotoxic T-lymphocyte epitope derived from HIV-1 Gag protein. AIDS 12: 2073-2074. – reference: McMichael AJ, Rowland-Jones SL. 2001. Cellular immune responses to HIV. Nature 410: 980-987. – reference: Oxenius A, Price DA, Gunthard HF, Dawson SJ, Fagard C, Perrin L, Fischer M, Weber R, Plana M, Garcia F, Hirschel B, McLean A, Phillips RE. 2002. Stimulation of HIV-specific cellular immunity by structured treatment interruption fails to enhance viral control in chronic HIV infection. Proc Natl Acad Sci USA 99: 13747-13752. – reference: Garcia F, Lejeune M, Climent N, Gil C, Alcami J, Morente V, Alos L, Ruiz A, Setoain J, Fumero E, Castro P, Lopez A, Cruceta A, Piera C, Florence E, Pereira A, Libois A, Gonzalez N, Guila M, Caballero M, Lomena F, Joseph J, Miro JM, Pumarola T, Plana M, Gatell JM, Gallart T. 2005. Therapeutic immunization with dendritic cells loaded with heat-inactivated autologous HIV-1 in patients with chronic HIV-1 infection. J Infect Dis 191: 1680-1685. – reference: Kuzushima K, Hayashi N, Kimura H, Tsurumi T. 2001. Efficient identification of HLA-A*2402-restricted cytomegalovirus-specific CD8+ T-cell epitopes by a computer algorithm and an enzyme-linked immunospot assay. Blood 98: 1872-1881. – reference: Tubiana R, Carcelain G, Vray M, Gourlain K, Dalban C, Chermak A, Rabian C, Vittecoq D, Simon A, Bouvet E, El Habib R, Costagliola D, Calvez V, Autran B, Katlama C, the Vacciter Study group. 2005. Therapeutic immunization with a human immunodeficiency virus (HIV) type 1-recombinant canarypox vaccine in chronically HIV-infected patients: The Vacciter Study (ANRS 094). Vaccine 23: 4292-4301. – reference: Foung SK, Taidi B, Ness D, Grumet FC. 1986. A monoclonal antibody against HLA-A11 and A24. Hum Immunol 15: 316-319. – reference: Tremblay CL, Hicks JL, Sutton L, Giguel F, Flynn T, Johnston M, Sax PE, Walker BD, Hirsch MS, Rosenberg ES, D'Aquila RT. 2003. Antiretroviral resistance associated with supervised treatment interruptions in treated acute HIV infection. AIDS 17: 1086-1089. – reference: Lisziewicz J, Trocio J, Xu J, Whitman L, Ryder A, Bakare N, Lewis MG, Wagner W, Pistorio A, Arya S, Lori F. 2005. Control of viral rebound through therapeutic immunization with DermaVir. AIDS 19: 35-43. – reference: Borrow P, Lewicki H, Hahn BH, Shaw GM, Oldstone MB. 1994. Virus-specific CD8 cytotoxic T-lymphocyte activity associated with control of viremia in primary human immunodeficiency virus type 1 infection. J Virol 68: 6103-6110. – reference: Kaufmann DE, Lichterfeld M, Altfeld M, Addo MM, Johnston MN, Lee PK, Wagner BS, Kalife ET, Strick D, Rosenberg ES, Walker BD. 2004. Limited durability of viral control following treated acute HIV infection. PLoS Med 1: e36. – reference: Lu W, Arraes LC, Ferreira WT, Andrieu JM. 2004. Therapeutic dendritic-cell vaccine for chronic HIV-1 infection. Nat Med 10: 1359-1365. – reference: Metzner KJ, Bonhoeffer S, Fischer M, Karanicolas R, Allers K, Joos B, Weber R, Hirschel B, Kostrikis LG, Gunthard HF, The Swiss HIV Cohort Study. 2003. Emergence of minor populations of human immunodeficiency virus type 1 carrying the M184V and L90M mutations in subjects undergoing structured treatment interruptions. J Infect Dis 188: 1433-1443. – reference: Bostrom AC, Hejdeman B, Matsuda R, Fredriksson M, Fredriksson EL, Bratt G, Sandstrom E, Wahren B. 2004. Long-term persistence of vaccination and HAART to human immunodeficiency virus (HIV). Vaccine 22: 1683-1691. – reference: Fagard C, Oxenius A, Gunthard H, Garcia F, Le Braz M, Mestre G, Battegay M, Furrer H, Vernazza P, Bernasconi E, Telenti A, Weber R, Leduc D, Yerly S, Price D, Dawson SJ, Klimkait T, Perneger TV, McLean A, Clotet B, Gatell JM, Perrin L, Plana M, Phillips R, Hirschel B, Swiss HIV Cohort Study. 2003. A prospective trial of structured treatment interruptions in human immunodeficiency virus infection. Arch Intern Med 163: 1220-1226. – reference: Ramratnam B, Mittler JE, Zhang L, Boden D, Hurley A, Fang F, Macken CA, Perelson AS, Markowitz M, Ho DD. 2000. The decay of the latent reservoir of replication-competent HIV-1 is inversely correlated with the extent of residual viral replication during prolonged anti-retroviral therapy. Nat Med 6: 82-85. – reference: Watanabe N, Tomizawa M, Tachikawa-Kawana A, Goto M, Ajisawa A, Nakamura T, Iwamoto A. 2001. Quantitative and qualitative abnormalities in HIV-1-specific T cells. AIDS 15: 711-715. – reference: Furutsuki T, Hosoya N, Kawana-Tachikawa A, Tomizawa M, Odawara T, Goto M, Kitamura Y, Nakamura T, Kelleher AD, Cooper DA, Iwamoto A. 2004. Frequent transmission of cytotoxic-T-lymphocyte escape mutants of human immunodeficiency virus type 1 in the highly HLA-A24-positive Japanese population. J Virol 78: 8437-8445. – reference: Banchereau J, Briere F, Caux C, Davoust J, Lebecque S, Liu YJ, Pulendran B, Palucka K. 2000. Immunobiology of dendritic cells. Annu Rev Immunol 18: 767-811. – reference: Banchereau J, Palucka AK. 2005. Dendritic cells as therapeutic vaccines against cancer. Nat Rev Immunol 5: 296-306. – reference: Harrer E, Bauerle M, Ferstl B, Chaplin P, Petzold B, Mateo L, Handley A, Tzatzaris M, Vollmar J, Bergmann S, Rittmaier M, Eismann K, Muller S, Kalden JR, Spriewald B, Willbold D, Harrer T. 2005. Therapeutic vaccination of HIV-1-infected patients on HAART with a recombinant HIV-1 nef-expressing MVA: Safety, immunogenicity and influence on viral load during treatment interruption. Antivir Ther 10: 285-300. – reference: Koup RA, Safrit JT, Cao Y, Andrews CA, McLeod G, Borkowsky W, Farthing C, Ho DD. 1994. Temporal association of cellular immune responses with the initial control of viremia in primary human immunodeficiency virus type 1 syndrome. J Virol 68: 4650-4655. – reference: Lange CG, Lederman MM, Medvik K, Asaad R, Wild M, Kalayjian R, Valdez H. 2003. Nadir CD4+ T-cell count and numbers of CD28+ CD4+ T-cells predict functional responses to immunizations in chronic HIV-1 infection. AIDS 17: 2015-2023. – reference: Schweighardt B, Ortiz GM, Grant RM, Wellons M, Miralles GD, Kostrikis LG, Bartlett JA, Nixon DF. 2002. Emergence of drug-resistant HIV-1 variants in patients undergoing structured treatment interruptions. AIDS 16: 2342-2344. – reference: Ikeda-Moore Y, Tomiyama H, Miwa K, Oka S, Iwamoto A, Kaneko Y, Takiguchi M. 1997. Identification and characterization of multiple HLA-A24-restricted HIV-1 CTL epitopes: Strong epitopes are derived from V regions of HIV-1. J Immunol 159: 6242-6252. – reference: Dorrell L, Dong T, Ogg GS, Lister S, McAdam S, Rostron T, Conlon C, McMichael AJ, Rowland-Jones SL. 1999. Distinct recognition of non-clade B human immunodeficiency virus type 1 epitopes by cytotoxic T lymphocytes generated from donors infected in Africa. J Virol 73: 1708-1714. – reference: Lee Sp, Tierney RJ, Thomas WA, Brooks JM, Rickinson AB. 1997. Conserved CTL epitopes within EBV latent membrane protein 2. J Immunol 158: 3325-3334. – reference: Siliciano JD, Kajdas J, Finzi D, Quinn TC, Chadwick K, Margolick JB, Kovacs C, Gange SJ, Siliciano RF. 2003. Long-term follow-up studies confirm the stability of the latent reservoir for HIV-1 in resting CD4+ T cells. Nat Med 9: 727-728. – volume: 16 start-page: 2342 year: 2002 end-page: 2344 article-title: Emergence of drug‐resistant HIV‐1 variants in patients undergoing structured treatment interruptions publication-title: AIDS – volume: 64 start-page: 4973 year: 2004 end-page: 4979 article-title: Vaccination with tumor lysate‐pulsed dendritic cells elicits antigen‐specific, cytotoxic T‐cells in patients with malignant glioma publication-title: Cancer Res – volume: 5 start-page: 296 year: 2005 end-page: 306 article-title: Dendritic cells as therapeutic vaccines against cancer publication-title: Nat Rev Immunol – volume: 15 start-page: 316 year: 1986 end-page: 319 article-title: A monoclonal antibody against HLA‐A11 and A24 publication-title: Hum Immunol – volume: 192 start-page: 607 year: 2005 end-page: 617 article-title: Impact of therapeutic immunization on HIV‐1 viremia after discontinuation of antiretroviral therapy initiated during acute infection publication-title: J Infect Dis – volume: 9 start-page: 727 year: 2003 end-page: 728 article-title: Long‐term follow‐up studies confirm the stability of the latent reservoir for HIV‐1 in resting CD4 T cells publication-title: Nat Med – volume: 68 start-page: 6103 year: 1994 end-page: 6110 article-title: Virus‐specific CD8 cytotoxic T‐lymphocyte activity associated with control of viremia in primary human immunodeficiency virus type 1 infection publication-title: J Virol – volume: 78 start-page: 8437 year: 2004 end-page: 8445 article-title: Frequent transmission of cytotoxic‐T‐lymphocyte escape mutants of human immunodeficiency virus type 1 in the highly HLA‐A24‐positive Japanese population publication-title: J Virol – volume: 159 start-page: 6242 year: 1997 end-page: 6252 article-title: Identification and characterization of multiple HLA‐A24‐restricted HIV‐1 CTL epitopes: Strong epitopes are derived from V regions of HIV‐1 publication-title: J Immunol – volume: 15 start-page: 711 year: 2001 end-page: 715 article-title: Quantitative and qualitative abnormalities in HIV‐1‐specific T cells publication-title: AIDS – volume: 98 start-page: 1872 year: 2001 end-page: 1881 article-title: Efficient identification of HLA‐A*2402‐restricted cytomegalovirus‐specific CD8 T‐cell epitopes by a computer algorithm and an enzyme‐linked immunospot assay publication-title: Blood – volume: 73 start-page: 1708 year: 1999 end-page: 1714 article-title: Distinct recognition of non‐clade B human immunodeficiency virus type 1 epitopes by cytotoxic T lymphocytes generated from donors infected in Africa publication-title: J Virol – volume: 68 start-page: 4650 year: 1994 end-page: 4655 article-title: Temporal association of cellular immune responses with the initial control of viremia in primary human immunodeficiency virus type 1 syndrome publication-title: J Virol – volume: 79 start-page: 8024 year: 2005 end-page: 8031 article-title: Enhanced breadth of CD4 T‐cell immunity by DNA prime and adenovirus boost immunization to human immunodeficiency virus Env and Gag immunogens publication-title: J Virol – volume: 18 start-page: 767 year: 2000 end-page: 811 article-title: Immunobiology of dendritic cells publication-title: Annu Rev Immunol – volume: 12 start-page: 2073 year: 1998 end-page: 2074 article-title: Identification of a novel HLA‐A24‐restricted cytotoxic T‐lymphocyte epitope derived from HIV‐1 Gag protein publication-title: AIDS – volume: 191 start-page: 1680 year: 2005 end-page: 1685 article-title: Therapeutic immunization with dendritic cells loaded with heat‐inactivated autologous HIV‐1 in patients with chronic HIV‐1 infection publication-title: J Infect Dis – volume: 10 start-page: 1359 year: 2004 end-page: 1365 article-title: Therapeutic dendritic‐cell vaccine for chronic HIV‐1 infection publication-title: Nat Med – volume: 410 start-page: 980 year: 2001 end-page: 987 article-title: Cellular immune responses to HIV publication-title: Nature – volume: 22 start-page: 1683 year: 2004 end-page: 1691 article-title: Long‐term persistence of vaccination and HAART to human immunodeficiency virus (HIV) publication-title: Vaccine – start-page: 139 year: 1996 end-page: 144 article-title: Report of the Japanese Central Bone Marrow Data Center publication-title: Clin Transpl – volume: 170 start-page: 4260 year: 2003 end-page: 4266 article-title: Decreased stimulation of CD4+ T cell proliferation and IL‐2 production by highly enriched populations of HIV‐infected dendritic cells publication-title: J Immunol – volume: 17 start-page: 1086 year: 2003 end-page: 1089 article-title: Antiretroviral resistance associated with supervised treatment interruptions in treated acute HIV infection publication-title: AIDS – volume: 23 start-page: 4292 year: 2005 end-page: 4301 article-title: Therapeutic immunization with a human immunodeficiency virus (HIV) type 1‐recombinant canarypox vaccine in chronically HIV‐infected patients: The Vacciter Study (ANRS 094) publication-title: Vaccine – volume: 158 start-page: 3325 year: 1997 end-page: 3334 article-title: Conserved CTL epitopes within EBV latent membrane protein 2 publication-title: J Immunol – volume: 6 start-page: 82 year: 2000 end-page: 85 article-title: The decay of the latent reservoir of replication‐competent HIV‐1 is inversely correlated with the extent of residual viral replication during prolonged anti‐retroviral therapy publication-title: Nat Med – volume: 163 start-page: 1220 year: 2003 end-page: 1226 article-title: A prospective trial of structured treatment interruptions in human immunodeficiency virus infection publication-title: Arch Intern Med – volume: 17 start-page: 2015 year: 2003 end-page: 2023 article-title: Nadir CD4 T‐cell count and numbers of CD28+ CD4+ T‐cells predict functional responses to immunizations in chronic HIV‐1 infection publication-title: AIDS – volume: 19 start-page: 35 year: 2005 end-page: 43 article-title: Control of viral rebound through therapeutic immunization with DermaVir publication-title: AIDS – volume: 99 start-page: 13747 year: 2002 end-page: 13752 article-title: Stimulation of HIV‐specific cellular immunity by structured treatment interruption fails to enhance viral control in chronic HIV infection publication-title: Proc Natl Acad Sci USA – volume: 10 start-page: 285 year: 2005 end-page: 300 article-title: Therapeutic vaccination of HIV‐1‐infected patients on HAART with a recombinant HIV‐1 nef‐expressing MVA: Safety, immunogenicity and influence on viral load during treatment interruption publication-title: Antivir Ther – volume: 188 start-page: 1433 year: 2003 end-page: 1443 article-title: Emergence of minor populations of human immunodeficiency virus type 1 carrying the M184V and L90M mutations in subjects undergoing structured treatment interruptions publication-title: J Infect Dis – volume: 4 start-page: 101 year: 2003 end-page: 110 article-title: Better preserved immune responses after immunization with rgp 160 in HIV‐1 infected patients treated with highly active antiretroviral therapy than in untreated patients with similar CD4 levels during at 2 years' follow‐up publication-title: HIV Med – volume: 1 start-page: e36 year: 2004 article-title: Limited durability of viral control following treated acute HIV infection publication-title: PLoS Med – ident: e_1_2_1_26_1 doi: 10.1073/pnas.202372199 – ident: e_1_2_1_27_1 doi: 10.1038/71577 – volume: 10 start-page: 285 year: 2005 ident: e_1_2_1_11_1 article-title: Therapeutic vaccination of HIV‐1‐infected patients on HAART with a recombinant HIV‐1 nef‐expressing MVA: Safety, immunogenicity and influence on viral load during treatment interruption publication-title: Antivir Ther doi: 10.1177/135965350501000212 – ident: e_1_2_1_19_1 doi: 10.1182/blood.V98.6.1872 – ident: e_1_2_1_8_1 doi: 10.1016/0198-8859(86)90006-6 – ident: e_1_2_1_20_1 doi: 10.1097/00002030-200309260-00002 – ident: e_1_2_1_2_1 doi: 10.1038/nri1592 – ident: e_1_2_1_29_1 doi: 10.1038/nm880 – volume: 68 start-page: 6103 year: 1994 ident: e_1_2_1_4_1 article-title: Virus‐specific CD8 cytotoxic T‐lymphocyte activity associated with control of viremia in primary human immunodeficiency virus type 1 infection publication-title: J Virol doi: 10.1128/jvi.68.9.6103-6110.1994 – ident: e_1_2_1_15_1 doi: 10.1371/journal.pmed.0010036 – ident: e_1_2_1_35_1 doi: 10.1158/0008-5472.CAN-03-3505 – ident: e_1_2_1_18_1 doi: 10.1128/JVI.68.7.4650-4655.1994 – ident: e_1_2_1_16_1 doi: 10.4049/jimmunol.170.8.4260 – ident: e_1_2_1_28_1 doi: 10.1097/00002030-200211220-00018 – ident: e_1_2_1_7_1 doi: 10.1001/archinte.163.10.1220 – ident: e_1_2_1_12_1 doi: 10.1046/j.1468-1293.2003.00148.x – ident: e_1_2_1_34_1 doi: 10.1128/JVI.79.13.8024-8031.2005 – ident: e_1_2_1_22_1 doi: 10.1097/00002030-200501030-00004 – ident: e_1_2_1_23_1 doi: 10.1038/nm1147 – start-page: 139 year: 1996 ident: e_1_2_1_30_1 article-title: Report of the Japanese Central Bone Marrow Data Center publication-title: Clin Transpl – volume: 73 start-page: 1708 year: 1999 ident: e_1_2_1_6_1 article-title: Distinct recognition of non‐clade B human immunodeficiency virus type 1 epitopes by cytotoxic T lymphocytes generated from donors infected in Africa publication-title: J Virol doi: 10.1128/JVI.73.2.1708-1714.1999 – volume: 159 start-page: 6242 year: 1997 ident: e_1_2_1_13_1 article-title: Identification and characterization of multiple HLA‐A24‐restricted HIV‐1 CTL epitopes: Strong epitopes are derived from V regions of HIV‐1 publication-title: J Immunol doi: 10.4049/jimmunol.159.12.6242 – ident: e_1_2_1_14_1 doi: 10.1097/00002030-199815000-00020 – ident: e_1_2_1_3_1 doi: 10.1146/annurev.immunol.18.1.767 – ident: e_1_2_1_9_1 doi: 10.1128/JVI.78.16.8437-8445.2004 – ident: e_1_2_1_25_1 doi: 10.1086/379215 – ident: e_1_2_1_32_1 doi: 10.1016/j.vaccine.2005.04.013 – ident: e_1_2_1_10_1 doi: 10.1086/429340 – ident: e_1_2_1_24_1 doi: 10.1038/35073658 – volume: 158 start-page: 3325 year: 1997 ident: e_1_2_1_21_1 article-title: Conserved CTL epitopes within EBV latent membrane protein 2 publication-title: J Immunol doi: 10.4049/jimmunol.158.7.3325 – ident: e_1_2_1_33_1 doi: 10.1097/00002030-200104130-00006 – ident: e_1_2_1_5_1 doi: 10.1016/j.vaccine.2003.09.049 – ident: e_1_2_1_17_1 doi: 10.1086/432002 – ident: e_1_2_1_31_1 doi: 10.1097/00002030-200305020-00021 |
SSID | ssj0008922 ssib004908942 ssib058493250 |
Score | 2.0676925 |
Snippet | Immune response enhanced by therapeutic HIV‐1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART).... Immune response enhanced by therapeutic HIV-1 vaccine may control viral proliferation after discontinuation of highly active antiretroviral therapy (HAART).... |
SourceID | proquest pubmed pascalfrancis crossref wiley nii istex |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 711 |
SubjectTerms | Adult Antiretroviral Therapy, Highly Active Biological and medical sciences CD4 Lymphocyte Count Chronic Disease Chronic Disease - therapy Dendritic Cells Dendritic Cells - immunology Dendritic Cells - metabolism Dendritic Cells - transplantation Drug Resistance, Viral Drug Resistance, Viral - genetics Epitopes, T-Lymphocyte Epitopes, T-Lymphocyte - immunology Fundamental and applied biological sciences. Psychology HAART HIV Antigens HIV Antigens - administration & dosage HIV Antigens - immunology HIV Infections HIV Infections - drug therapy HIV Infections - immunology HIV Infections - therapy HIV-1 HIV-1 - drug effects HIV-1 - genetics HIV-1 - immunology Human immunodeficiency virus 1 Human viral diseases Humans Immunotherapy Immunotherapy - methods Infectious diseases Male Medical sciences Microbiology Middle Aged Miscellaneous Mutation T-Lymphocytes, Cytotoxic T-Lymphocytes, Cytotoxic - immunology treatment interruption vaccine Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids Viral Load Virology |
Title | Peptide-loaded dendritic-cell vaccination followed by treatment interruption for chronic HIV-1 infection: A phase 1 trial |
URI | https://api.istex.fr/ark:/67375/WNG-G48GLR61-N/fulltext.pdf https://cir.nii.ac.jp/crid/1871709542524873728 https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmv.20612 https://www.ncbi.nlm.nih.gov/pubmed/16628588 https://www.proquest.com/docview/20550923 https://www.proquest.com/docview/67901505 |
Volume | 78 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaqIiEuvKFpabEQQr2kzcNxHDhViO5SsStU0dIDUuRXRGnJrrK75XGBn8Bv5JcwYye7WtRKiEsURZM4tseeb-zxN4Q8TZnJYqFZaITk6KBkIRhBGfJKSTAYOqk0OoqDIe8fsYOT7GSFvOjOwnh-iPmCG44MN1_jAJdqsrsgDf30-QLcO-4yDGOsFgKiwwV1lCj8DgLMBCHYoKxjFYqS3fmbS7boGjbrVzAx9ekpRkjKCTRS5bNbXAY_l9GsM0f7t8iHriI-CuVsZzZVO_r7XxyP_1nT2-RmC1PpnterO2TF1nfJ9UG7EX-P_HiL0TDG_v7563wkjTUU5i_j0ibAI9wNoBdSg6zreFqBto2-gJT6Rueh7RSpKppmNm5FGqo9Uy_tvz6Gr8S0ixSrn9M9Ov4IBpfG1OUZuU-O9l-9e9kP21wOoc4AI4G_K3WUqzRlyhq4Vyqy8DwrDEC23CZcRBqgmIyVFJKlVcWt4JoLR3CmACc-IKv1qLZrhLJCAEyNI5FrwWJpZGzw_JhRrOAFYzIg212vlrolOsd8G-elp2hOSmjQ0jVoQJ7MRcee3eMyoWdONeYSsjnDcLg8K98Pe2WPid6bQx6Xw4Bsgu5AmXiNwRPNAb_CnJiAU5jmiQjI1pJWLYrMkUNIFAF53KlZCaMcO0vWdjSbwI-AJwlY_GoJnrvFqywgD71-Lr7O8ZisgOK3nZZdXdPyYHDsbtb_XXSD3PCrUrgw9YisTpuZ3QScNlVbbkD-AR6yN3s |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V3LbtNAFL0qrQRseD8MtB0hQN24jZ3xeIzEoqI0SZtEqOprZ-ZlUVqcKI-WsoFP4EP4FX6CL-HO2E4U1EpsumBjWdbVjMf3Pb5zLsCLOtVRwBX1NRfMJiiRj05Q-CyTAh2GCjNlE8VOlzX36NZhdDgHP6uzMAU-xGTDzWqGs9dWwe2G9NoUNfTT51PM79BDlyWV2-b8DBO24ZvWBnL3ZRhuvtt92_TLngK-itBXY94lVC2W9TqVRuO9lDWDz6NEY-gQm5DxmsKQQARScEHrWcYMZ4pxB7QlMV7Bca_Bgu0gbpH6N3amYFU8Kf5ZoO3x0etFFY5RLVybvOqM91uwjPyCTi0_OrI1mWKIbMmKfhoXBbyz8bNzgJu34Vf16Yq6l-PV8Uiuqq9_oUr-L9_2DtwqI3GyXqjOXZgz-T243ilrDe7Dt_e24Eeb399_nPSENpqgidauMwQ-sj88yKlQSOtkm2SoUL0zpJLnZFK9Tywax2Aw7pckA6IKMGLSbO3jKAGpiuHy12Sd9D9iTEEC4lqpPIC9K1n-Q5jPe7l5DIQmHCPxoMZjxWkgtAi0PSKnJU1YQqnwYKUSo1SVWO62pchJWqBQhykyMHUM9OD5hLRfAJhcRPTKyeKEQgyObcVfHKUH3UbaoLzR3mFB2vVgEYUV57TXAJPtGEN0NPsh5r31OOQeLM2I8XTK2MIk8cSD5UquUzRkllkiN73xEF8Ek2VMNy6nYLHbn4s8eFQoxHR0Zk8Cc5x-xYn15StNtzr77ubJv5Muw43mbqedtlvd7adws9iEs_twz2B-NBibRQxLR3LJWQMCH65aRf4AtjeT1A |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V3LbtQwFL0qrVSxKW8aoK2FAHWTNsk4joPEomKYR9sZVRV97IJjO6K0ZEbzaCkb-AT-g1_hK_gSrp1kRoNaiU0XbKIourLj3LdzfS7AixpVoc8ldRUXzCQooYtOULgsSwU6DBlk0iSKnS5rHdDt4_B4Dn5WZ2EKfIjJhpvRDGuvjYL3VbY5BQ399Pkc0zt00GVF5Y6-vMB8bfimXUfmvgyCxrv3b1tu2VLAlSG6aky7hPSitFajqVZ4n6aexudhrDByiHTAuCcxIhB-KrigtSxjmjPJuMXZSjFcwXFvwQJlXmz6RNT3p1hVPC5-WaDpcdHphRWMkRdsTl51xvktGD5-QZ-Wn5yYkkwxRK5kRTuNq-Ld2fDZ-r_GHfhVfbmi7OV0YzxKN-TXv0Al_5NPexeWyjicbBWKcw_mdH4fFjtlpcED-LZnyn2U_v39x1lPKK0IGmhl-0LgI_O7g5wLibRWskmG6tS7QKr0kkxq94nB4hgMxv2SZEBkAUVMWu1DHMUnVSlc_ppskf5HjCiIT2wjlYdwcCPLfwTzeS_Xy0BozDEO9z0eSU59oYSvzAE5ldKYxZQKB9YrKUpkieRuGoqcJQUGdZAgAxPLQAeeT0j7BXzJVUSvrChOKMTg1NT7RWFy1G0mTcqbu_vMT7oOrKCs4pzm6mOqHWGAjkY_wKy3FgXcgdUZKZ5OGRmQJB47sFaJdYJmzDBL5Lo3HuKLYKqMycb1FCyyu3OhA48LfZiOzsw5YI7Tr1upvn6lyXbn0N48-XfSNVjcqzeS3XZ35yncLnbgzCbcM5gfDcZ6BWPSUbpqbQGBDzetIX8AVNySgw |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Peptide-loaded+dendritic-cell+vaccination+followed+by+treatment+interruption+for+chronic+HIV-1+infection%3A+a+phase+1+trial&rft.jtitle=Journal+of+medical+virology&rft.au=Ide%2C+Fuyuaki&rft.au=Nakamura%2C+Tetsuya&rft.au=Tomizawa%2C+Mariko&rft.au=Kawana-Tachikawa%2C+Ai&rft.date=2006-06-01&rft.issn=0146-6615&rft.volume=78&rft.issue=6&rft.spage=711&rft_id=info:doi/10.1002%2Fjmv.20612&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0146-6615&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0146-6615&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0146-6615&client=summon |