Effects of HTLV-1 on leukocyte trafficking and migration in ACs compared to healthy individuals

Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 h...

Full description

Saved in:
Bibliographic Details
Published inBMC research notes Vol. 17; no. 1; pp. 222 - 6
Main Authors Letafati, Arash, Bahavar, Atefeh, Norouzi, Mehdi, Rasouli, Aziz, Hedayatyaghoubi, Mojtaba, Molaverdi, Ghazale, Mozhgani, Sayed-Hamidreza, Siami, Zeinab
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 10.08.2024
BioMed Central
BMC
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 has been implicated in the development of several disorders that mimic auto-inflammation. T-cell migration is important topic in the context of HTLV-1 associated diseases progression. The primary objective of this case-control study was to assess the relationship between increased mRNA expression in virus migration following HTLV-1 infection. PBMCs from 20 asymptomatic patients and 20 healthy subjects were analyzed using real-time PCR to measure mRNA expression of LFA1, MLCK, RAC1, RAPL, ROCK1, VAV1 and CXCR4. Also, mRNA expression of Tax and HBZ were evaluated. Mean expression of Tax and HBZ in ACs (asymptomatic carriers) was 0.7218 and 0.6517 respectively. The results revealed a noteworthy upregulation of these genes involved in T-cell migration among ACs patients in comparison to healthy individuals. Considering the pivotal role of gene expression alterations associated with the progression into two major diseases (ATLL or HAM/TSP), analyzing the expression of these genes in the ACs group can offer probable potential diagnostic markers and aid in monitoring the condition of ACs.
AbstractList Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 has been implicated in the development of several disorders that mimic auto-inflammation. T-cell migration is important topic in the context of HTLV-1 associated diseases progression. The primary objective of this case-control study was to assess the relationship between increased mRNA expression in virus migration following HTLV-1 infection. PBMCs from 20 asymptomatic patients and 20 healthy subjects were analyzed using real-time PCR to measure mRNA expression of LFA1, MLCK, RAC1, RAPL, ROCK1, VAV1 and CXCR4. Also, mRNA expression of Tax and HBZ were evaluated. Mean expression of Tax and HBZ in ACs (asymptomatic carriers) was 0.7218 and 0.6517 respectively. The results revealed a noteworthy upregulation of these genes involved in T-cell migration among ACs patients in comparison to healthy individuals. Considering the pivotal role of gene expression alterations associated with the progression into two major diseases (ATLL or HAM/TSP), analyzing the expression of these genes in the ACs group can offer probable potential diagnostic markers and aid in monitoring the condition of ACs.Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 has been implicated in the development of several disorders that mimic auto-inflammation. T-cell migration is important topic in the context of HTLV-1 associated diseases progression. The primary objective of this case-control study was to assess the relationship between increased mRNA expression in virus migration following HTLV-1 infection. PBMCs from 20 asymptomatic patients and 20 healthy subjects were analyzed using real-time PCR to measure mRNA expression of LFA1, MLCK, RAC1, RAPL, ROCK1, VAV1 and CXCR4. Also, mRNA expression of Tax and HBZ were evaluated. Mean expression of Tax and HBZ in ACs (asymptomatic carriers) was 0.7218 and 0.6517 respectively. The results revealed a noteworthy upregulation of these genes involved in T-cell migration among ACs patients in comparison to healthy individuals. Considering the pivotal role of gene expression alterations associated with the progression into two major diseases (ATLL or HAM/TSP), analyzing the expression of these genes in the ACs group can offer probable potential diagnostic markers and aid in monitoring the condition of ACs.
Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 has been implicated in the development of several disorders that mimic auto-inflammation. T-cell migration is important topic in the context of HTLV-1 associated diseases progression. The primary objective of this case–control study was to assess the relationship between increased mRNA expression in virus migration following HTLV-1 infection. PBMCs from 20 asymptomatic patients and 20 healthy subjects were analyzed using real-time PCR to measure mRNA expression of LFA1, MLCK, RAC1, RAPL, ROCK1, VAV1 and CXCR4. Also, mRNA expression of Tax and HBZ were evaluated. Mean expression of Tax and HBZ in ACs (asymptomatic carriers) was 0.7218 and 0.6517 respectively. The results revealed a noteworthy upregulation of these genes involved in T-cell migration among ACs patients in comparison to healthy individuals. Considering the pivotal role of gene expression alterations associated with the progression into two major diseases (ATLL or HAM/TSP), analyzing the expression of these genes in the ACs group can offer probable potential diagnostic markers and aid in monitoring the condition of ACs.
Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 has been implicated in the development of several disorders that mimic auto-inflammation. T-cell migration is important topic in the context of HTLV-1 associated diseases progression. The primary objective of this case-control study was to assess the relationship between increased mRNA expression in virus migration following HTLV-1 infection. PBMCs from 20 asymptomatic patients and 20 healthy subjects were analyzed using real-time PCR to measure mRNA expression of LFA1, MLCK, RAC1, RAPL, ROCK1, VAV1 and CXCR4. Also, mRNA expression of Tax and HBZ were evaluated. Mean expression of Tax and HBZ in ACs (asymptomatic carriers) was 0.7218 and 0.6517 respectively. The results revealed a noteworthy upregulation of these genes involved in T-cell migration among ACs patients in comparison to healthy individuals. Considering the pivotal role of gene expression alterations associated with the progression into two major diseases (ATLL or HAM/TSP), analyzing the expression of these genes in the ACs group can offer probable potential diagnostic markers and aid in monitoring the condition of ACs.
Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 has been implicated in the development of several disorders that mimic auto-inflammation. T-cell migration is important topic in the context of HTLV-1 associated diseases progression. The primary objective of this case–control study was to assess the relationship between increased mRNA expression in virus migration following HTLV-1 infection. PBMCs from 20 asymptomatic patients and 20 healthy subjects were analyzed using real-time PCR to measure mRNA expression of LFA1, MLCK, RAC1, RAPL, ROCK1, VAV1 and CXCR4. Also, mRNA expression of Tax and HBZ were evaluated. Mean expression of Tax and HBZ in ACs (asymptomatic carriers) was 0.7218 and 0.6517 respectively. The results revealed a noteworthy upregulation of these genes involved in T-cell migration among ACs patients in comparison to healthy individuals. Considering the pivotal role of gene expression alterations associated with the progression into two major diseases (ATLL or HAM/TSP), analyzing the expression of these genes in the ACs group can offer probable potential diagnostic markers and aid in monitoring the condition of ACs.
Abstract Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 has been implicated in the development of several disorders that mimic auto-inflammation. T-cell migration is important topic in the context of HTLV-1 associated diseases progression. The primary objective of this case–control study was to assess the relationship between increased mRNA expression in virus migration following HTLV-1 infection. PBMCs from 20 asymptomatic patients and 20 healthy subjects were analyzed using real-time PCR to measure mRNA expression of LFA1, MLCK, RAC1, RAPL, ROCK1, VAV1 and CXCR4. Also, mRNA expression of Tax and HBZ were evaluated. Mean expression of Tax and HBZ in ACs (asymptomatic carriers) was 0.7218 and 0.6517 respectively. The results revealed a noteworthy upregulation of these genes involved in T-cell migration among ACs patients in comparison to healthy individuals. Considering the pivotal role of gene expression alterations associated with the progression into two major diseases (ATLL or HAM/TSP), analyzing the expression of these genes in the ACs group can offer probable potential diagnostic markers and aid in monitoring the condition of ACs.
Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases, including adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Aside from HAM/TSP, HTLV-1 has been implicated in the development of several disorders that mimic auto-inflammation. T-cell migration is important topic in the context of HTLV-1 associated diseases progression. The primary objective of this case-control study was to assess the relationship between increased mRNA expression in virus migration following HTLV-1 infection. PBMCs from 20 asymptomatic patients and 20 healthy subjects were analyzed using real-time PCR to measure mRNA expression of LFA1, MLCK, RAC1, RAPL, ROCK1, VAV1 and CXCR4. Also, mRNA expression of Tax and HBZ were evaluated. Mean expression of Tax and HBZ in ACs (asymptomatic carriers) was 0.7218 and 0.6517 respectively. The results revealed a noteworthy upregulation of these genes involved in T-cell migration among ACs patients in comparison to healthy individuals. Considering the pivotal role of gene expression alterations associated with the progression into two major diseases (ATLL or HAM/TSP), analyzing the expression of these genes in the ACs group can offer probable potential diagnostic markers and aid in monitoring the condition of ACs. Keywords: HTLV-1, ACs, Cell migration, ATLL, HAM/TSP, MRNA expression
ArticleNumber 222
Audience Academic
Author Norouzi, Mehdi
Mozhgani, Sayed-Hamidreza
Letafati, Arash
Rasouli, Aziz
Molaverdi, Ghazale
Siami, Zeinab
Hedayatyaghoubi, Mojtaba
Bahavar, Atefeh
Author_xml – sequence: 1
  givenname: Arash
  surname: Letafati
  fullname: Letafati, Arash
– sequence: 2
  givenname: Atefeh
  surname: Bahavar
  fullname: Bahavar, Atefeh
– sequence: 3
  givenname: Mehdi
  surname: Norouzi
  fullname: Norouzi, Mehdi
– sequence: 4
  givenname: Aziz
  surname: Rasouli
  fullname: Rasouli, Aziz
– sequence: 5
  givenname: Mojtaba
  surname: Hedayatyaghoubi
  fullname: Hedayatyaghoubi, Mojtaba
– sequence: 6
  givenname: Ghazale
  surname: Molaverdi
  fullname: Molaverdi, Ghazale
– sequence: 7
  givenname: Sayed-Hamidreza
  surname: Mozhgani
  fullname: Mozhgani, Sayed-Hamidreza
– sequence: 8
  givenname: Zeinab
  surname: Siami
  fullname: Siami, Zeinab
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39127702$$D View this record in MEDLINE/PubMed
BookMark eNptkl1v0zAUhiM0xD7gD3CBInEDFxl27CTOFaqqwSpV2s3YrXXqj9RdEhfbmei_53QdY0XIik9kP35z8vo9z05GP5ose0_JJaWi_hIpo4QXpMSnFqIpqlfZGW2quiAVIScv3k-z8xg3hNRUCPomO2UtLZuGlGeZvLLWqBRzb_Pr2-VdQXM_5r2Z7r3aJZOnANY6de_GLodR54PrAiSHjBvz2Tzmyg9bCEbnyedrA31a73BLuwenJ-jj2-y1xWLePdWL7Me3q9v5dbG8-b6Yz5aFqnibClYJrlea1qbBCo3SpBVQ6hrqUlAcVWu5ZSswNaMtE3XbNLQhNasoTqplF9nioKs9bOQ2uAHCTnpw8nHBh05CSE71RgI3LSgtqIaWW1ED2shLsgJOStoCQa2vB63ttBqMVmZEF_oj0eOd0a1l5x8kRSXsjKHCpyeF4H9OJiY5uKhM38No_BQlI3gBohF83_jHf9CNn8KIXh2oljFa_qU6wD9wo_X4YbUXlTNBOEdX2L7xy_9QOLQZnMLwWIfrRwc-Hx1AJplfqYMpRrm4uTtmP7x05dmOP1lCoDwAKvgYg7HPCCVyH1h5CKzEwMrHwMqK_QbZXtiq
Cites_doi 10.1083/jcb.130.3.613
10.1089/088922299310728
10.1007/s10911-007-9046-4
10.1016/j.it.2012.07.004
10.1038/onc.2015.508
10.1002/cphy.c110012
10.1111/j.1750-3639.2007.00067.x
10.3727/096368914X685258
10.1074/jbc.M502639200
10.1016/j.imlet.2004.02.008
10.1186/1478-811X-11-50
10.1128/JVI.00443-10
10.3389/fphys.2018.01942
10.4049/jimmunol.180.2.931
10.3389/fimmu.2018.00952
10.1016/j.bbadis.2018.05.002
10.1002/iub.598
10.1172/JCI29226
10.1016/0165-6147(96)10033-X
10.3390/cancers9110153
10.20892/j.issn.2095-3941.2016.0086
10.1002/JLB.2MR1217-494R
10.1016/j.tips.2012.04.002
10.1016/j.molimm.2009.01.014
10.2174/156652413804486296
10.1038/s41419-018-0641-7
10.1016/j.virol.2012.09.028
10.1016/j.bbcan.2015.07.003
10.1128/MCB.20.19.7160-7169.2000
10.1084/jem.20011663
10.1186/s13027-023-00492-0
10.1016/S0165-2478(02)00236-5
10.1038/sj.onc.1208978
ContentType Journal Article
Copyright 2024. The Author(s).
COPYRIGHT 2024 BioMed Central Ltd.
2024. This work is licensed under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
The Author(s) 2024 2024
Copyright_xml – notice: 2024. The Author(s).
– notice: COPYRIGHT 2024 BioMed Central Ltd.
– notice: 2024. This work is licensed under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: The Author(s) 2024 2024
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
IOV
3V.
7X7
7XB
88E
8FE
8FH
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
HCIFZ
K9.
LK8
M0S
M1P
M7P
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.1186/s13104-024-06887-5
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Gale In Context: Opposing Viewpoints
ProQuest Central (Corporate)
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
ProQuest SciTech Collection
ProQuest Natural Science Journals
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One
ProQuest Central
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
ProQuest SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
Biological Sciences
ProQuest Health & Medical Collection
Medical Database
Biological Science Database
ProQuest Central Premium
ProQuest One Academic (New)
ProQuest Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Central China
ProQuest Central
ProQuest One Applied & Life Sciences
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Health & Medical Research Collection
Biological Science Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Biological Science Collection
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
Publicly Available Content Database

MEDLINE




Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  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: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 4
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Biology
EISSN 1756-0500
EndPage 6
ExternalDocumentID oai_doaj_org_article_a4e9acd81da94f86a131420ba40219a0
PMC11316973
A804463130
39127702
10_1186_s13104_024_06887_5
Genre Journal Article
GeographicLocations Iran
Germany
GeographicLocations_xml – name: Iran
– name: Germany
GroupedDBID ---
0R~
23N
2WC
53G
5GY
5VS
6J9
7X7
88E
8FE
8FH
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAYXX
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACMJI
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AEAQA
AFKRA
AFPKN
AHBYD
AHMBA
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BBNVY
BCNDV
BENPR
BFQNJ
BHPHI
BMC
BPHCQ
BVXVI
C6C
CCPQU
CITATION
CS3
DIK
E3Z
EBD
EBLON
EBS
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HCIFZ
HMCUK
HYE
IAO
IEA
IHR
INH
INR
IOV
ITC
KQ8
LGEZI
LK8
LOTEE
M1P
M48
M7P
MK0
M~E
NADUK
NXXTH
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
RBZ
RNS
ROL
RPM
RSV
SBL
SOJ
SV3
TR2
TUS
UKHRP
~8M
-A0
3V.
ACRMQ
ADINQ
C24
CGR
CUY
CVF
ECM
EIF
NPM
PMFND
7XB
8FK
AZQEC
DWQXO
GNUQQ
K9.
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQUKI
PRINS
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c549t-3584dbd16e74dba7cd098a2d6a628181859f4f3bae63193869771706351063c93
IEDL.DBID M48
ISSN 1756-0500
IngestDate Wed Aug 27 01:32:34 EDT 2025
Thu Aug 21 18:31:50 EDT 2025
Tue Aug 05 10:33:55 EDT 2025
Fri Jul 25 19:12:20 EDT 2025
Tue Jun 17 22:05:09 EDT 2025
Tue Jun 10 21:03:58 EDT 2025
Fri Jun 27 05:52:11 EDT 2025
Wed Feb 19 02:05:38 EST 2025
Tue Jul 01 02:00:18 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords ACs
HAM/TSP
MRNA expression
HTLV-1
ATLL
Cell migration
Language English
License 2024. The Author(s).
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c549t-3584dbd16e74dba7cd098a2d6a628181859f4f3bae63193869771706351063c93
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1186/s13104-024-06887-5
PMID 39127702
PQID 3091293312
PQPubID 55247
PageCount 6
ParticipantIDs doaj_primary_oai_doaj_org_article_a4e9acd81da94f86a131420ba40219a0
pubmedcentral_primary_oai_pubmedcentral_nih_gov_11316973
proquest_miscellaneous_3091287849
proquest_journals_3091293312
gale_infotracmisc_A804463130
gale_infotracacademiconefile_A804463130
gale_incontextgauss_IOV_A804463130
pubmed_primary_39127702
crossref_primary_10_1186_s13104_024_06887_5
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2024-08-10
PublicationDateYYYYMMDD 2024-08-10
PublicationDate_xml – month: 08
  year: 2024
  text: 2024-08-10
  day: 10
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: London
PublicationTitle BMC research notes
PublicationTitleAlternate BMC Res Notes
PublicationYear 2024
Publisher BioMed Central Ltd
BioMed Central
BMC
Publisher_xml – name: BioMed Central Ltd
– name: BioMed Central
– name: BMC
References Y-L Zhang (6887_CR22) 2017; 14
S Man (6887_CR9) 2007; 17
LF Reynolds (6887_CR27) 2002; 195
W Mothes (6887_CR6) 2010; 84
G-B Li (6887_CR33) 2013; 11
Y Zhao (6887_CR34) 2012; 64
AA Bhat (6887_CR18) 2019; 9
A Shayeghpour (6887_CR11) 2023; 18
K Hieshima (6887_CR5) 2008; 180
K Kohama (6887_CR17) 1996; 17
PA Gagliardi (6887_CR30) 2015; 1856
M Reina (6887_CR12) 2017; 9
SL Goodman (6887_CR15) 2012; 33
T Kinashi (6887_CR24) 2004; 93
R Zhang (6887_CR32) 2018; 9
M Moriuchi (6887_CR37) 1999; 15
C-Y Lin (6887_CR19) 2015; 24
ZM Goeckeler (6887_CR16) 1995; 130
JM Laufer (6887_CR23) 2018; 104
K Noma (6887_CR35) 2008; 118
C Hu (6887_CR31) 2019; 55
B Engelhardt (6887_CR10) 2012; 33
BP Liu (6887_CR25) 2000; 20
B Poon (6887_CR7) 1997
D Kedrin (6887_CR8) 2007; 12
M Nejmeddine (6887_CR21) 2005; 280
F Valderrama (6887_CR26) 2012; 125
R Grassmann (6887_CR1) 2005; 24
BL Walling (6887_CR13) 2018; 9
AR Thomsen (6887_CR3) 2003; 85
VB Shah (6887_CR28) 2009; 46
J Montalvo (6887_CR29) 2013; 13
LB Cook (6887_CR2) 2013; 435
X Trepat (6887_CR4) 2012; 2
D Kim (6887_CR20) 2016; 35
M Moriuchi (6887_CR36) 1999; 20
W Shen (6887_CR14) 2018; 1864
References_xml – volume: 130
  start-page: 613
  issue: 3
  year: 1995
  ident: 6887_CR16
  publication-title: J Cell Biol
  doi: 10.1083/jcb.130.3.613
– volume: 15
  start-page: 821
  issue: 9
  year: 1999
  ident: 6887_CR37
  publication-title: AIDS Res Hum Retrovir
  doi: 10.1089/088922299310728
– volume: 12
  start-page: 143
  year: 2007
  ident: 6887_CR8
  publication-title: J Mammary Gland Biol Neoplasia
  doi: 10.1007/s10911-007-9046-4
– volume-title: Virus–host interactions of human retroviruses
  year: 1997
  ident: 6887_CR7
– volume: 33
  start-page: 579
  issue: 12
  year: 2012
  ident: 6887_CR10
  publication-title: Trends Immunol
  doi: 10.1016/j.it.2012.07.004
– volume: 35
  start-page: 4495
  issue: 34
  year: 2016
  ident: 6887_CR20
  publication-title: Oncogene
  doi: 10.1038/onc.2015.508
– volume: 55
  start-page: 833
  issue: 4
  year: 2019
  ident: 6887_CR31
  publication-title: Int J Oncol
– volume: 2
  start-page: 2369
  issue: 4
  year: 2012
  ident: 6887_CR4
  publication-title: Compr Physiol
  doi: 10.1002/cphy.c110012
– volume: 17
  start-page: 243
  issue: 2
  year: 2007
  ident: 6887_CR9
  publication-title: Brain Pathol
  doi: 10.1111/j.1750-3639.2007.00067.x
– volume: 24
  start-page: 2011
  issue: 10
  year: 2015
  ident: 6887_CR19
  publication-title: Cell Transplant
  doi: 10.3727/096368914X685258
– volume: 280
  start-page: 29653
  issue: 33
  year: 2005
  ident: 6887_CR21
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M502639200
– volume: 93
  start-page: 1
  issue: 1
  year: 2004
  ident: 6887_CR24
  publication-title: RAPL Immunol Lett
  doi: 10.1016/j.imlet.2004.02.008
– volume: 11
  start-page: 1
  issue: 1
  year: 2013
  ident: 6887_CR33
  publication-title: Cell Commun Signaling
  doi: 10.1186/1478-811X-11-50
– volume: 84
  start-page: 8360
  issue: 17
  year: 2010
  ident: 6887_CR6
  publication-title: J Virol
  doi: 10.1128/JVI.00443-10
– volume: 9
  start-page: 1942
  year: 2019
  ident: 6887_CR18
  publication-title: Front Physiol
  doi: 10.3389/fphys.2018.01942
– volume: 180
  start-page: 931
  issue: 2
  year: 2008
  ident: 6887_CR5
  publication-title: J Immunol
  doi: 10.4049/jimmunol.180.2.931
– volume: 9
  start-page: 952
  year: 2018
  ident: 6887_CR13
  publication-title: Front Immunol
  doi: 10.3389/fimmu.2018.00952
– volume: 1864
  start-page: 2566
  issue: 8
  year: 2018
  ident: 6887_CR14
  publication-title: Biochim Biophys Acta (BBA) Mol Basis Dis
  doi: 10.1016/j.bbadis.2018.05.002
– volume: 64
  start-page: 194
  issue: 2
  year: 2012
  ident: 6887_CR34
  publication-title: IUBMB Life
  doi: 10.1002/iub.598
– volume: 118
  start-page: 1632
  issue: 5
  year: 2008
  ident: 6887_CR35
  publication-title: J Clin Investig
  doi: 10.1172/JCI29226
– volume: 17
  start-page: 284
  issue: 8
  year: 1996
  ident: 6887_CR17
  publication-title: Trends Pharmacol Sci
  doi: 10.1016/0165-6147(96)10033-X
– volume: 20
  start-page: A77
  issue: 4
  year: 1999
  ident: 6887_CR36
  publication-title: JAIDS J Acquir Immune Defic Syndr
– volume: 9
  start-page: 153
  issue: 11
  year: 2017
  ident: 6887_CR12
  publication-title: Cancers
  doi: 10.3390/cancers9110153
– volume: 14
  start-page: 90
  issue: 1
  year: 2017
  ident: 6887_CR22
  publication-title: Cancer Biol Med
  doi: 10.20892/j.issn.2095-3941.2016.0086
– volume: 104
  start-page: 301
  issue: 2
  year: 2018
  ident: 6887_CR23
  publication-title: J Leukoc Biol
  doi: 10.1002/JLB.2MR1217-494R
– volume: 33
  start-page: 405
  issue: 7
  year: 2012
  ident: 6887_CR15
  publication-title: Trends Pharmacol Sci
  doi: 10.1016/j.tips.2012.04.002
– volume: 46
  start-page: 1845
  issue: 8–9
  year: 2009
  ident: 6887_CR28
  publication-title: Mol Immunol
  doi: 10.1016/j.molimm.2009.01.014
– volume: 13
  start-page: 205
  issue: 1
  year: 2013
  ident: 6887_CR29
  publication-title: Curr Mol Med
  doi: 10.2174/156652413804486296
– volume: 9
  start-page: 598
  issue: 6
  year: 2018
  ident: 6887_CR32
  publication-title: Cell Death Dis
  doi: 10.1038/s41419-018-0641-7
– volume: 435
  start-page: 131
  issue: 1
  year: 2013
  ident: 6887_CR2
  publication-title: Virology
  doi: 10.1016/j.virol.2012.09.028
– volume: 1856
  start-page: 178
  issue: 2
  year: 2015
  ident: 6887_CR30
  publication-title: Biochim Biophys Acta (BBA) Rev Cancer
  doi: 10.1016/j.bbcan.2015.07.003
– volume: 125
  start-page: 3310
  issue: 14
  year: 2012
  ident: 6887_CR26
  publication-title: J Cell Sci
– volume: 20
  start-page: 7160
  issue: 19
  year: 2000
  ident: 6887_CR25
  publication-title: Mol Cell Biol
  doi: 10.1128/MCB.20.19.7160-7169.2000
– volume: 195
  start-page: 1103
  issue: 9
  year: 2002
  ident: 6887_CR27
  publication-title: J Exp Med
  doi: 10.1084/jem.20011663
– volume: 18
  start-page: 1
  issue: 1
  year: 2023
  ident: 6887_CR11
  publication-title: Infect Agents Cancer
  doi: 10.1186/s13027-023-00492-0
– volume: 85
  start-page: 119
  issue: 2
  year: 2003
  ident: 6887_CR3
  publication-title: Immunol Lett
  doi: 10.1016/S0165-2478(02)00236-5
– volume: 24
  start-page: 5976
  issue: 39
  year: 2005
  ident: 6887_CR1
  publication-title: Oncogene
  doi: 10.1038/sj.onc.1208978
SSID ssj0061881
Score 2.3620684
Snippet Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases,...
Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases,...
Abstract Human T-lymphotropic virus type 1 (HTLV-1) is a RNA virus belonging to Retroviridae family and is associated with the development of various diseases,...
SourceID doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
StartPage 222
SubjectTerms ACs
Adult
Adult T-cell leukemia-lymphoma
Analysis
Asymptomatic
ATLL
Basic-Leucine Zipper Transcription Factors
Case-Control Studies
Cell adhesion & migration
Cell migration
Cell Movement
Central nervous system diseases
CXCR4 protein
Development and progression
Female
Gene expression
Gene Products, tax - genetics
Genes
Genetic aspects
HAM/TSP
Health aspects
Hereditary spastic paraplegia
HTLV-1
HTLV-I Infections - genetics
HTLV-I Infections - immunology
HTLV-I Infections - virology
Human T-lymphotropic virus 1 - genetics
Human T-lymphotropic virus 1 - physiology
Humans
Infections
Inflammation
Kinases
Leukocyte migration
Leukocytes
Leukocytes - immunology
Leukocytes - metabolism
Lymphocyte Function-Associated Antigen-1 - genetics
Lymphocyte Function-Associated Antigen-1 - metabolism
Lymphocytes
Lymphocytes T
Lymphoma
Male
Males
Metastasis
Middle Aged
Motility
MRNA expression
Myosin-light-chain kinase
Nervous system
Proteins
Proto-Oncogene Proteins c-vav - genetics
Proto-Oncogene Proteins c-vav - metabolism
Rac1 protein
Receptors, CXCR4 - genetics
Receptors, CXCR4 - metabolism
Research Note
Retroviridae Proteins
rho-Associated Kinases - genetics
rho-Associated Kinases - metabolism
Risk factors
RNA viruses
RNA, Messenger - genetics
RNA, Messenger - metabolism
Spinal cord
Tropical spastic paraparesis
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQpUpcEG8CpTIIiQOKmsReP47bqtWCeFzaqjfL8aOsCgki2cP-e2biZLURBy6cIsXjKPnGk5lJZj4T8g6U7CHpcjkrCp9z73RuI-cQyEmmIjgN67HB-ctXsbrin24WN3tbfWFNWKIHTsCdWB60dR7CKqt5VMKWrORVUVtIfEpth2wdfN6UTKV3sCiVKqcWGSVOOpiE1RYVHzZZkfli5oYGtv6_38l7TmleMLnngS4ekgdj6EiX6ZYfkXuheUwO02aS2yfEJCLijraRri4_X-clbRv6I2zuWrftA4VLIl0EfhqntvH05_o2aZ-uG7o86-hUjk77lqb2yC1d7_q1uqfk6uL88myVj9sn5A6Svj5nEFv42pciSDha6Xyhla28sAIpoMBR68gjq20QYIdMCQgFkUyHgZkK5jR7Rg6atgkvCOWSxSjxu6PTXMVaRYmRkw6FrmpuZUY-TGiaX4klwwzZhRImYW8AezNgbxYZOUXAd5LIcD2cAL2bUe_mX3rPyFtUl0EOiwaLZG7tpuvMx2_XZqnwLzUD75yR96NQbAFlZ8eeA3gqpL2aSR7NJMHI3Hx4WhVmNPLOMFh3EC2xssrIm90wzsTCtSa0m1FGScV1Rp6nRbR7bgZDUhYwW82W1wyY-Uiz_j5QgJeABuiLvfwfUL4i96vBNJDo94gc9L834TWEWn19PFjVH2V-IiY
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lj9QwDI5gERIXxJvCggJC4oCqbZtMHic0rFgNiMdldzW3KM1jdgS0y7ZzmH-P3RdbIXGq1LhV49ixndqfCXkDi-wh6HIpyzKfcu90aiPn4MhJpiIYDeuxwPnrN7E645_Xi_Vw4NYMaZXjntht1L52eEZ-xMCwgWliefH-8neKXaPw7-rQQuMmuYXQZZjSJddTwCVypfKxUEaJoyYHX4anYJW6VisyXcyMUYfZ_-_OfM00zdMmr9mhk3vk7uBA0mW_4vfJjVA9ILf7lpL7h8T0cMQNrSNdnX45T3NaV_Rn2P2o3b4NFF6JoBF4QE5t5emv7aaXAbqt6PK4oWNSOm1r2hdJ7ul2qtpqHpGzk4-nx6t0aKKQOgj92pSBh-FLn4sg4Wql85lWtvDCCgSCAnOtI4-stEGANjIlwCFESB0GyiqY0-wxOajqKjwllEsWo8TTR6e5iqWKEv0nHTJdlNzKhLwbuWkue6wM08UYSpie9wZ4bzrem0VCPiDDJ0rEue5u1FcbM6iNsTxo6zw41VbzqISF1_AiKy2Evbm2WUJe43IZRLKoMFVmY3dNYz59PzdLhf-qGdjohLwdiGINXHZ2qDyAWSH41YzycEYJqubmw6NUmEHVG_NXMBPyahrGJzF9rQr1bqBRUnGdkCe9EE3zZjAkZQZPq5l4zRgzH6m2Fx0QeA7cgPViz_7_Xc_JnaITegTyPSQH7dUuvABXqi1fdvryBxnyGa8
  priority: 102
  providerName: ProQuest
Title Effects of HTLV-1 on leukocyte trafficking and migration in ACs compared to healthy individuals
URI https://www.ncbi.nlm.nih.gov/pubmed/39127702
https://www.proquest.com/docview/3091293312
https://www.proquest.com/docview/3091287849
https://pubmed.ncbi.nlm.nih.gov/PMC11316973
https://doaj.org/article/a4e9acd81da94f86a131420ba40219a0
Volume 17
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3db9MwED_tQ0i8IL7JGJVBSDygQBK7_nhAqJs2lYoNBOvUN8v5cKnYEmhaif73nJ2kWsTEU6T4YjXnu97vHN_vAF7jIueYdGUhjaI8ZHmmQmMZQyAnqLQYNEzuCpzPzvl4yiaz4WwHunZHrQLrW1M7109qurx69-f35iM6_Afv8JK_r2PEKCzEaONbqIhwuAv7GJmEc9Qztv2qwGPpm5ZixMQsehhFXRHNrXP0ApXn8__3X_tG2OofqbwRo07vw70WXJJRYw0PYKcoH8Kdpt3k5hHohqq4JpUl44vPl2FMqpJcFeufVbZZFQSndIQSbvOcmDIn14t5Yx9kUZLRcU26A-tkVZGmgHJDFtuKrvoxTE9PLo7HYdtgIcwwLVyFFNFHnuYxLwRejcjySEmT5NxwRxKFoVxZZmlqCo6eSiVHsOjodig6MqeZok9gr6zK4hkQJqi1wu1MZopJm0orHLZSRaSSlBkRwNtOm_pXw6Ohff4huW50r1H32uteDwM4cgrfSjoObH-jWs5161LasEKZLEfAbRSzkhuchiVRajAljpWJAnjllks7lovSHaOZm3Vd609fLvVIuu_YFON3AG9aIVuhljPTViXgWzlirJ7kYU8S3TDrD3dWoTsr1hTRGOIpGicBvNwOuyfd0bayqNatjBSSqQCeNka0fW-KQ0JE-LTsmVdPMf2RcvHDk4THqA1cL3rw_5_9HO4m3ugdye8h7K2W6-IFwqxVOoBdMRMD2B-NJt8neD06Of_6beA3LQber_4CcUUjcA
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1bb9MwFLamTgheEHcCAwwC8YCiJbFrOw8IdWNTy7qCUDftzTi-lApIxpIK9U_xGznOpSxC4m1PleKTqDk-V-ec7yD0EjbZQNKlQxJFJqRGp6FylEIgx4lw4DSU8Q3OxzM2PqEfzoZnW-h31wvjyyo7m1gbalNof0a-S8CxgWsicfLu_Gfop0b5r6vdCI1GLI7s-hekbOXbyXvY31dJcngw3x-H7VSBUEMuVIUEXK7JTMwsh1_FtYlSoRLDFPPISOC_UkcdyZRlIJ5EMIiQPMYMAellRHvwJTD525RAKjNA23sHs0-fO9vPYiHirjVHsN0yhuiJhuAH6-EuPBz23F89JeBfX3DJGfYLNS95vsNb6GYbsuJRI2O30ZbN76BrzRDL9V0kGwDkEhcOj-fT0zDGRY6_29W3Qq8ri-GRHqbCH8ljlRv8Y7lopA4vczzaL3FXBo-rAjdtmWu83PSJlffQyZUw-D4a5EVuHyJMOXGO-_NOnVLhMuG4j9hSG6VJRhUP0JuOm_K8QeeQdVYjmGx4L4H3sua9HAZozzN8Q-mRtesLxcVCtooqFbWp0gbCeJVSJ5iCx9AkyhQk2nGqogC98NslPXZG7otzFmpVlnLy8VSOhP86TiAqCNDrlsgVwGWt2l4HeCsPt9Wj3OlRgnLr_nInFbI1LqX8qwoBer5Z9nf6grncFquWRnBB0wA9aIRo894EljiP4G7RE68eY_or-fJrDT0eAzdgv8ij__-vZ-j6eH48ldPJ7OgxupHUCuBhhHfQoLpY2ScQyFXZ01Z7MPpy1Qr7B4E2Vaw
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=Effects+of+HTLV-1+on+leukocyte+trafficking+and+migration+in+ACs+compared+to+healthy+individuals&rft.jtitle=BMC+research+notes&rft.au=Letafati%2C+Arash&rft.au=Bahavar%2C+Atefeh&rft.au=Norouzi%2C+Mehdi&rft.au=Rasouli%2C+Aziz&rft.date=2024-08-10&rft.pub=BioMed+Central+Ltd&rft.issn=1756-0500&rft.eissn=1756-0500&rft.volume=17&rft.issue=1&rft_id=info:doi/10.1186%2Fs13104-024-06887-5&rft.externalDocID=A804463130
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1756-0500&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1756-0500&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1756-0500&client=summon