Phenotypic and Functional Profiles of Antigen-Specific CD4+ and CD8+ T Cells Associated With Infection Control in Patients With Cutaneous Leishmaniasis
The host immunological response is a key factor determining the pathogenesis of cutaneous leishmaniasis. It is known that a Th1 cellular response is associated with infection control and that antigen-specific memory T cells are necessary for the development of a rapid and strong protective cellular...
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Published in | Frontiers in cellular and infection microbiology Vol. 8; p. 393 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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19.11.2018
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Abstract | The host immunological response is a key factor determining the pathogenesis of cutaneous leishmaniasis. It is known that a Th1 cellular response is associated with infection control and that antigen-specific memory T cells are necessary for the development of a rapid and strong protective cellular response. The present manuscript reports the analysis of the functional and phenotypic profiles of antigen-specific CD4
and CD8
T cells from patients cured of cutaneous leishmaniasis (CL), patients with an active process of cutaneous leishmaniasis, asymptomatic individuals with a positive Montenegro test and healthy donors (HD). Peripheral blood mononuclear cells (PBMCs) from the patients exhibited a lymphoproliferative capacity after stimulation with total soluble protein from either
(S
A) or
(S
A) or with a recombinant paraflagellar rod protein-1 (rPFR1). Higher frequencies of antigen-specific T
cells, mainly following stimulation with rPFR1, were observed in asymptomatic and cured patients than in patients with active cutaneous leishmaniasis, while T cells from patients with active cutaneous leishmaniasis showed a higher percentage of effector memory T cells (T
for CD4
T cells and T
for CD8
T cells). The amount of antigen-specific CD57
/CD8
T
cells in patients with active cutaneous leishmaniasis was higher than that in cured patients and asymptomatic subjects. Regarding functionality, a more robust multifunctional CD8
T cell response was detected in cured patients than in those with active cutaneous leishmaniasis. Moreover, cured patients showed a significant increase in the frequency of cells expressing a Th1-type cytotoxic production profile (IFN-γ
/granzyme-B/
perforin
). Patients with an active leishmaniosis process had a significantly higher frequency of CD8
T cells expressing the inhibitory CD160 and 2B4 receptors than did cured patients. The expression profile observed in cured patients could be indicative of an imbalance toward a CD8
Th1 response, which could be associated with infection control; consequently, the determination of this profile could be a useful tool for facilitating the clinical follow-up of patients with cutaneous leishmaniasis. The results also suggest a possible exhaustion process of CD8
T cells associated with the evolution of
infection. |
---|---|
AbstractList | The host immunological response is a key factor determining the pathogenesis of cutaneous leishmaniasis. It is known that a Th1 cellular response is associated with infection control and that antigen-specific memory T cells are necessary for the development of a rapid and strong protective cellular response. The present manuscript reports the analysis of the functional and phenotypic profiles of antigen-specific CD4+ and CD8+ T cells from patients cured of cutaneous leishmaniasis (CL), patients with an active process of cutaneous leishmaniasis, asymptomatic individuals with a positive Montenegro test and healthy donors (HD). Peripheral blood mononuclear cells (PBMCs) from the patients exhibited a lymphoproliferative capacity after stimulation with total soluble protein from either Leishmania panamensis (SLpA) or Leishmania infantum (SLiA) or with a recombinant paraflagellar rod protein-1 (rPFR1). Higher frequencies of antigen-specific TNAIVE cells, mainly following stimulation with rPFR1, were observed in asymptomatic and cured patients than in patients with active cutaneous leishmaniasis, while T cells from patients with active cutaneous leishmaniasis showed a higher percentage of effector memory T cells (TEM for CD4+ T cells and TEMRA for CD8+ T cells). The amount of antigen-specific CD57+/CD8+ TEMRA cells in patients with active cutaneous leishmaniasis was higher than that in cured patients and asymptomatic subjects. Regarding functionality, a more robust multifunctional CD8+ T cell response was detected in cured patients than in those with active cutaneous leishmaniasis. Moreover, cured patients showed a significant increase in the frequency of cells expressing a Th1-type cytotoxic production profile (IFN-γ+/granzyme-B/+perforin+). Patients with an active leishmaniosis process had a significantly higher frequency of CD8+ T cells expressing the inhibitory CD160 and 2B4 receptors than did cured patients. The expression profile observed in cured patients could be indicative of an imbalance toward a CD8+ Th1 response, which could be associated with infection control; consequently, the determination of this profile could be a useful tool for facilitating the clinical follow-up of patients with cutaneous leishmaniasis. The results also suggest a possible exhaustion process of CD8+ T cells associated with the evolution of Leishmania infection.The host immunological response is a key factor determining the pathogenesis of cutaneous leishmaniasis. It is known that a Th1 cellular response is associated with infection control and that antigen-specific memory T cells are necessary for the development of a rapid and strong protective cellular response. The present manuscript reports the analysis of the functional and phenotypic profiles of antigen-specific CD4+ and CD8+ T cells from patients cured of cutaneous leishmaniasis (CL), patients with an active process of cutaneous leishmaniasis, asymptomatic individuals with a positive Montenegro test and healthy donors (HD). Peripheral blood mononuclear cells (PBMCs) from the patients exhibited a lymphoproliferative capacity after stimulation with total soluble protein from either Leishmania panamensis (SLpA) or Leishmania infantum (SLiA) or with a recombinant paraflagellar rod protein-1 (rPFR1). Higher frequencies of antigen-specific TNAIVE cells, mainly following stimulation with rPFR1, were observed in asymptomatic and cured patients than in patients with active cutaneous leishmaniasis, while T cells from patients with active cutaneous leishmaniasis showed a higher percentage of effector memory T cells (TEM for CD4+ T cells and TEMRA for CD8+ T cells). The amount of antigen-specific CD57+/CD8+ TEMRA cells in patients with active cutaneous leishmaniasis was higher than that in cured patients and asymptomatic subjects. Regarding functionality, a more robust multifunctional CD8+ T cell response was detected in cured patients than in those with active cutaneous leishmaniasis. Moreover, cured patients showed a significant increase in the frequency of cells expressing a Th1-type cytotoxic production profile (IFN-γ+/granzyme-B/+perforin+). Patients with an active leishmaniosis process had a significantly higher frequency of CD8+ T cells expressing the inhibitory CD160 and 2B4 receptors than did cured patients. The expression profile observed in cured patients could be indicative of an imbalance toward a CD8+ Th1 response, which could be associated with infection control; consequently, the determination of this profile could be a useful tool for facilitating the clinical follow-up of patients with cutaneous leishmaniasis. The results also suggest a possible exhaustion process of CD8+ T cells associated with the evolution of Leishmania infection. The host immunological response is a key factor determining the pathogenesis of cutaneous leishmaniasis. It is known that a Th1 cellular response is associated with infection control and that antigen-specific memory T cells are necessary for the development of a rapid and strong protective cellular response. The present manuscript reports the analysis of the functional and phenotypic profiles of antigen-specific CD4 and CD8 T cells from patients cured of cutaneous leishmaniasis (CL), patients with an active process of cutaneous leishmaniasis, asymptomatic individuals with a positive Montenegro test and healthy donors (HD). Peripheral blood mononuclear cells (PBMCs) from the patients exhibited a lymphoproliferative capacity after stimulation with total soluble protein from either (S A) or (S A) or with a recombinant paraflagellar rod protein-1 (rPFR1). Higher frequencies of antigen-specific T cells, mainly following stimulation with rPFR1, were observed in asymptomatic and cured patients than in patients with active cutaneous leishmaniasis, while T cells from patients with active cutaneous leishmaniasis showed a higher percentage of effector memory T cells (T for CD4 T cells and T for CD8 T cells). The amount of antigen-specific CD57 /CD8 T cells in patients with active cutaneous leishmaniasis was higher than that in cured patients and asymptomatic subjects. Regarding functionality, a more robust multifunctional CD8 T cell response was detected in cured patients than in those with active cutaneous leishmaniasis. Moreover, cured patients showed a significant increase in the frequency of cells expressing a Th1-type cytotoxic production profile (IFN-γ /granzyme-B/ perforin ). Patients with an active leishmaniosis process had a significantly higher frequency of CD8 T cells expressing the inhibitory CD160 and 2B4 receptors than did cured patients. The expression profile observed in cured patients could be indicative of an imbalance toward a CD8 Th1 response, which could be associated with infection control; consequently, the determination of this profile could be a useful tool for facilitating the clinical follow-up of patients with cutaneous leishmaniasis. The results also suggest a possible exhaustion process of CD8 T cells associated with the evolution of infection. The host immunological response is a key factor determining the pathogenesis of cutaneous leishmaniasis. It is known that a Th1 cellular response is associated with infection control and that antigen-specific memory T cells are necessary for the development of a rapid and strong protective cellular response. The present manuscript reports the analysis of the functional and phenotypic profiles of antigen-specific CD4 + and CD8 + T cells from patients cured of cutaneous leishmaniasis (CL), patients with an active process of cutaneous leishmaniasis, asymptomatic individuals with a positive Montenegro test and healthy donors (HD). Peripheral blood mononuclear cells (PBMCs) from the patients exhibited a lymphoproliferative capacity after stimulation with total soluble protein from either Leishmania panamensis (S Lp A) or Leishmania infantum (S Li A) or with a recombinant paraflagellar rod protein-1 (rPFR1). Higher frequencies of antigen-specific T NAIVE cells, mainly following stimulation with rPFR1, were observed in asymptomatic and cured patients than in patients with active cutaneous leishmaniasis, while T cells from patients with active cutaneous leishmaniasis showed a higher percentage of effector memory T cells (T EM for CD4 + T cells and T EMRA for CD8 + T cells). The amount of antigen-specific CD57 + /CD8 + T EMRA cells in patients with active cutaneous leishmaniasis was higher than that in cured patients and asymptomatic subjects. Regarding functionality, a more robust multifunctional CD8 + T cell response was detected in cured patients than in those with active cutaneous leishmaniasis. Moreover, cured patients showed a significant increase in the frequency of cells expressing a Th1-type cytotoxic production profile (IFN-γ + /granzyme-B/ + perforin + ). Patients with an active leishmaniosis process had a significantly higher frequency of CD8 + T cells expressing the inhibitory CD160 and 2B4 receptors than did cured patients. The expression profile observed in cured patients could be indicative of an imbalance toward a CD8 + Th1 response, which could be associated with infection control; consequently, the determination of this profile could be a useful tool for facilitating the clinical follow-up of patients with cutaneous leishmaniasis. The results also suggest a possible exhaustion process of CD8 + T cells associated with the evolution of Leishmania infection. The host immunological response is a key factor determining the pathogenesis of cutaneous leishmaniasis. It is known that a Th1 cellular response is associated with infection control and that antigen-specific memory T cells are necessary for the development of a rapid and strong protective cellular response. The present manuscript reports the analysis of the functional and phenotypic profiles of antigen-specific CD4+ and CD8+ T cells from patients cured of cutaneous leishmaniasis (CL), patients with an active process of cutaneous leishmaniasis, asymptomatic individuals with a positive Montenegro test and healthy donors (HD). Peripheral blood mononuclear cells (PBMCs) from the patients exhibited a lymphoproliferative capacity after stimulation with total soluble protein from either Leishmania panamensis (SLpA) or Leishmania infantum (SLiA) or with a recombinant paraflagellar rod protein-1 (rPFR1). Higher frequencies of antigen-specific TNAIVE cells, mainly following stimulation with rPFR1, were observed in asymptomatic and cured patients than in patients with active cutaneous leishmaniasis, while T cells from patients with active cutaneous leishmaniasis showed a higher percentage of effector memory T cells (TEM for CD4+ T cells and TEMRA for CD8+ T cells). The amount of antigen-specific CD57+/CD8+ TEMRA cells in patients with active cutaneous leishmaniasis was higher than that in cured patients and asymptomatic subjects. Regarding functionality, a more robust multifunctional CD8+ T cell response was detected in cured patients than in those with active cutaneous leishmaniasis. Moreover, cured patients showed a significant increase in the frequency of cells expressing a Th1-type cytotoxic production profile (IFN-γ+/granzyme-B/+perforin+). Patients with an active leishmaniosis process had a significantly higher frequency of CD8+ T cells expressing the inhibitory CD160 and 2B4 receptors than did cured patients. The expression profile observed in cured patients could be indicative of an imbalance toward a CD8+ Th1 response, which could be associated with infection control; consequently, the determination of this profile could be a useful tool for facilitating the clinical follow-up of patients with cutaneous leishmaniasis. The results also suggest a possible exhaustion process of CD8+ T cells associated with the evolution of Leishmania infection. |
Author | Gómez, Inmaculada Infante, Juan José Pérez-Antón, Elena Robledo, Sara María Ledesma, Darién Vélez, Ivan Darío López, Manuel C. Egui, Adriana Thomas, M. Carmen Montoya, Andrés |
AuthorAffiliation | 3 Bionaturis Group, Bioorganic Research and Services, S.A. , Jerez de la Frontera , Spain 2 Programa de Estudio y Control de Enfermedades Tropicales, Facultad de Medicina, Universidad de Antioquia , Medellín , Colombia 1 Molecular Biology Department, Instituto de Parasitología y Biomedicina “López Neyra”, Consejo Superior de Investigaciones Científicas , Granada , Spain |
AuthorAffiliation_xml | – name: 3 Bionaturis Group, Bioorganic Research and Services, S.A. , Jerez de la Frontera , Spain – name: 2 Programa de Estudio y Control de Enfermedades Tropicales, Facultad de Medicina, Universidad de Antioquia , Medellín , Colombia – name: 1 Molecular Biology Department, Instituto de Parasitología y Biomedicina “López Neyra”, Consejo Superior de Investigaciones Científicas , Granada , Spain |
Author_xml | – sequence: 1 givenname: Adriana surname: Egui fullname: Egui, Adriana – sequence: 2 givenname: Darién surname: Ledesma fullname: Ledesma, Darién – sequence: 3 givenname: Elena surname: Pérez-Antón fullname: Pérez-Antón, Elena – sequence: 4 givenname: Andrés surname: Montoya fullname: Montoya, Andrés – sequence: 5 givenname: Inmaculada surname: Gómez fullname: Gómez, Inmaculada – sequence: 6 givenname: Sara María surname: Robledo fullname: Robledo, Sara María – sequence: 7 givenname: Juan José surname: Infante fullname: Infante, Juan José – sequence: 8 givenname: Ivan Darío surname: Vélez fullname: Vélez, Ivan Darío – sequence: 9 givenname: Manuel C. surname: López fullname: López, Manuel C. – sequence: 10 givenname: M. Carmen surname: Thomas fullname: Thomas, M. Carmen |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30510917$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1371/journal.pntd.0002567 10.1002/eji.201040384 10.1371/journal.pone.0035671 10.1128/IAI.62.6.2614-2618.1994 10.1086/340261 10.1590/S0074-02762007000100013 10.1016/S0035-9203(02)90071-4 10.1007/s10875-012-9788-7 10.7705/biomedica.v26i1.1508 10.1371/journal.pone.0122115 10.1038/35065118 10.1007/s12026-008-8016-2 10.1111/j.1365-2133.2005.06647.x 10.1038/nm1108 10.1016/j.celrep.2014.06.012 10.1038/srep28266 10.4049/jimmunol.1202537 10.1016/0140-6736(90)91945-7 10.1038/nrmicro2608 10.1128/AAC.04298-14 10.7705/biomedica.v28i4.66 10.1128/IAI.59.8.2839-2842.1991 10.1189/jlb.0208107 10.1186/s12917-017-1224-z 10.1016/j.virol.2014.12.033 10.3389/fpubh.2014.00165 10.1016/S0166-6851(97)00149-7 10.1128/CDLI.9.2.251-256.2002 10.1093/infdis/jit401 10.1016/0248-4900(88)90056-1 10.1590/S0100-879X1998000100019 10.1016/j.trstmh.2006.02.014 10.1371/journal.ppat.1000431 10.3390/ijms18081742 10.1128/IAI.62.3.837-842.1994 10.1038/nri933 10.1016/j.imbio.2016.03.007 10.1371/journal.pntd.0001204 10.1016/j.cellimm.2016.07.010 10.1128/IAI.61.1.220-226.1993 10.1128/IAI.02404-14 10.1371/journal.pntd.0000871 10.4049/jimmunol.1602095 10.4049/jimmunol.166.6.4012 10.1086/382135 10.1016/j.vaccine.2006.07.006 10.1086/600109 10.1111/cei.12798 10.1371/journal.pntd.0000512 10.1084/jem.20030159 10.3389/fimmu.2018.01021 10.1590/S0100-879X1998000100020 10.1038/jid.2013.4 10.1128/IAI.71.6.3165-3171.2003 10.1128/JCM.29.4.757-763.1991 10.1111/j.1365-3024.2007.00991.x 10.4269/ajtmh.1990.42.206 10.1155/2014/636039 10.1111/j.1365-3024.2009.01125.x 10.4049/jimmunol.1500459 10.1007/s40257-015-0114-z 10.1371/journal.pntd.0004178 10.1002/eji.200939451 10.1371/journal.ppat.1003504 10.3389/fimmu.2016.00151 10.4049/jimmunol.1301810 10.1111/j.1365-3024.2009.01116.x 10.1016/j.molimm.2012.05.021 10.1016/j.micinf.2012.02.006 10.1146/annurev.immunol.22.012703.104702 10.1002/eji.200535458 10.1016/j.pt.2012.07.001 |
ContentType | Journal Article |
Copyright | Copyright © 2018 Egui, Ledesma, Pérez-Antón, Montoya, Gómez, Robledo, Infante, Vélez, López and Thomas. 2018 Egui, Ledesma, Pérez-Antón, Montoya, Gómez, Robledo, Infante, Vélez, López and Thomas |
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Keywords | phenotype Th1-cytokines paraflagellar rod protein-1 Leishmania biomarkers inhibitory receptors CD8+ and CD4+ T-cells leishmaniasis |
Language | English |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Parasite and Host, a section of the journal Frontiers in Cellular and Infection Microbiology Reviewed by: Hira Nakhasi, Center for Biologics Evaluation and Research (FDA), United States; Javier Moreno, Instituto de Salud Carlos III, Spain; Vicente Larraga, Department of Cellular and Molecular Biology, Consejo Superior de Investigaciones Científicas (CSIC), Spain Edited by: Eugenia Carrillo, Instituto de Salud Carlos III, Spain |
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References | Ramírez (B57) 2016; 6 Barroso (B5) 2018; 9 Michailowsky (B48) 2003; 71 Von Stebut (B69) 2003; 198 Esch (B24) 2013; 191 Naouar (B52) 2014; 2014 Ruiz (B61) 2007; 29 Sallusto (B63) 2004; 22 Aebischer (B1) 1993; 61 Chattopadhyay (B10) 2009; 85 de Vries (B21) 2015; 16 Arias (B3) 2014; 8 Jayakumar (B33) 2011; 5 Mateus (B45) 2017; 198 Corredor (B12) 1990; 42 Ledesma (B43) 2017; 13 Santrich (B65) 1997; 90 Zaph (B73) 2004; 10 Khamesipour (B38) 2012; 14 B70 De Luca (B18) 2016; 7 Egui (B23) 2012; 52 Hernández-Ruiz (B32) 2010; 4 Robinson (B59) 2002; 96 Alvar (B2) 2012; 7 Morell (B50) 2006; 24 Okwor (B54) 2008; 41 Castilho (B8) 2010; 40 Pinheiro (B56) 2007; 102 Santos Cda (B64) 2013; 133 Mou (B51) 2013; 190 Rodrigues (B60) 2014; 8 Coutinho (B13) 1998; 31 Gigley (B30) 2012; 28 Novais (B53) 2013; 9 Sacks (B62) 2002; 2 Cachon (B6) 1988; 63 Follador (B28) 2002; 34 Ovalle (B55) 2006; 26 da Silva Santos (B14) 2014; 2 Xu (B72) 2017; 18 Fiuza (B27) 2009; 3 Saravia (B66) 1990; 336 Lakhal-Naouar (B40) 2015; 9 Laskay (B41) 1991; 29 Bangham (B4) 2009; 39 Chiku (B11) 2016; 221 Kip (B39) 2015; 59 Cardoso (B7) 2015; 83 Silveira (B67) 2009; 31 Kahan (B35) 2015; 480 Da-Cruz (B17) 1994; 62 Lasso (B42) 2015; 195 de Oliveira Camera (B19) 2006; 100 Keshavarz Valian (B37) 2013; 33 Ribeiro-de-Jesus (B58) 1998; 31 Joshi (B34) 2009; 5 Da-Cruz (B15) 2005; 153 Champagne (B9) 2001; 410 Melby (B46) 1994; 62 Mendonça (B47) 2004; 189 Egui (B22) 2015; 10 de Oliveira Mendes-Aguiar (B20) 2016; 185 Kaye (B36) 2011; 9 Gautam (B29) 2014; 209 Da-Cruz (B16) 2002; 9 Faria (B25) 2009; 31 Montalvo (B49) 2008; 28 Wilhelm (B71) 2001; 166 Figueroa (B26) 2009; 200 Glennie (B31) 2016; 309 Theodos (B68) 1991; 59 Liang (B44) 2006; 36 |
References_xml | – volume: 8 start-page: e2567 year: 2014 ident: B60 article-title: Impairment of T cell function in parasitic infections publication-title: PLoS Negl. Trop. Dis doi: 10.1371/journal.pntd.0002567 – volume: 40 start-page: 2816 year: 2010 ident: B8 article-title: Murine model of chronic L. (Viannia) panamensis infection: role of IL-13 in disease publication-title: Eur. J. Immunol doi: 10.1002/eji.201040384 – volume: 7 start-page: e35671 year: 2012 ident: B2 article-title: Leishmaniasis worldwide and global estimates of its incidence publication-title: PLoS ONE doi: 10.1371/journal.pone.0035671 – volume: 62 start-page: 2614 year: 1994 ident: B17 article-title: Leishmania-reactive CD4+ and CD8+ T cells associated with cure of human cutaneous leishmaniasis publication-title: Infect. Immun doi: 10.1128/IAI.62.6.2614-2618.1994 – volume: 34 start-page: E54 year: 2002 ident: B28 article-title: Epidemiologic and immunologic findings for the subclinical form of Leishmania braziliensis infection publication-title: Clin. Infect. Dis doi: 10.1086/340261 – volume: 102 start-page: 79 year: 2007 ident: B56 article-title: Interferon-gamma is required for the late but not early control of Leishmania amazonensis infection in C57Bl/6 mice publication-title: Mem. Inst. Oswaldo Cruz doi: 10.1590/S0074-02762007000100013 – volume: 96 start-page: S169 year: 2002 ident: B59 article-title: The method used to sample ulcers influences the diagnosis of cutaneous Leishmaniasis publication-title: Trans. R. Soc. Trop. Med. Hyg doi: 10.1016/S0035-9203(02)90071-4 – volume: 33 start-page: 220 year: 2013 ident: B37 article-title: CCR7+ central and CCR7- effector memory CD4+ T cells in human cutaneous leishmaniasis publication-title: J. Clin. Immunol doi: 10.1007/s10875-012-9788-7 – volume: 26 start-page: 145 year: 2006 ident: B55 article-title: [Geographic distribution of Leishmania species isolated from patients at the National Institute of Dermatology Federico Lleras Acosta E.S.E., 1995-2005] publication-title: Biomedica doi: 10.7705/biomedica.v26i1.1508 – volume: 10 start-page: e0122115 year: 2015 ident: B22 article-title: Differential phenotypic and functional profiles of TcCA-2 -specific cytotoxic CD8+ T cells in the asymptomatic versus cardiac phase in Chagasic patients publication-title: PLoS ONE doi: 10.1371/journal.pone.0122115 – volume: 410 start-page: 106 year: 2001 ident: B9 article-title: Skewed maturation of memory HIV-specific CD8 T lymphocytes publication-title: Nature doi: 10.1038/35065118 – volume: 41 start-page: 123 year: 2008 ident: B54 article-title: Persistent parasites and immunologic memory in cutaneous leishmaniasis: implications for vaccine designs and vaccination strategies publication-title: Immunol. Res doi: 10.1007/s12026-008-8016-2 – volume: 153 start-page: 537 year: 2005 ident: B15 article-title: Flow cytometric analysis of cellular infiltrate from American tegumentary leishmaniasis lesions publication-title: Br. J. Dermatol doi: 10.1111/j.1365-2133.2005.06647.x – volume: 10 start-page: 1104 year: 2004 ident: B73 article-title: Central memory T cells mediate long-term immunity to Leishmania major in the absence of persistent parasites publication-title: Nat. Med doi: 10.1038/nm1108 – volume: 8 start-page: 420 year: 2014 ident: B3 article-title: Elucidating sources and roles of granzymes A and B during bacterial infection and sepsis publication-title: Cell Rep doi: 10.1016/j.celrep.2014.06.012 – volume: 6 start-page: 28266 year: 2016 ident: B57 article-title: Taxonomy, diversity, temporal and geographical distribution of Cutaneous Leishmaniasis in Colombia: a retrospective study publication-title: Sci. Rep doi: 10.1038/srep28266 – volume: 190 start-page: 3380 year: 2013 ident: B51 article-title: Parasite-derived arginase influences secondary anti-Leishmania immunity by regulating programmed cell death-1-mediated CD4+ T cell exhaustion publication-title: J. Immunol doi: 10.4049/jimmunol.1202537 – volume: 336 start-page: 398 year: 1990 ident: B66 article-title: Recurrent lesions in human Leishmania braziliensis infection–reactivation or reinfection? publication-title: Lancet doi: 10.1016/0140-6736(90)91945-7 – volume: 9 start-page: 604 year: 2011 ident: B36 article-title: Leishmaniasis: complexity at the host-pathogen interface publication-title: Nat. Rev. Microbiol doi: 10.1038/nrmicro2608 – volume: 59 start-page: 1 year: 2015 ident: B39 article-title: Systematic review of biomarkers to monitor therapeutic response in leishmaniasis publication-title: Antimicrob. Agents Chemother doi: 10.1128/AAC.04298-14 – volume: 28 start-page: 597 year: 2008 ident: B49 article-title: [PCR-RFLP and RAPD for typing neotropical Leishmania] publication-title: Biomedica doi: 10.7705/biomedica.v28i4.66 – volume: 59 start-page: 2839 year: 1991 ident: B68 article-title: Role of tumor necrosis factor in macrophage leishmanicidal activity in vitro and resistance to cutaneous leishmaniasis in vivo publication-title: Infect. Immun doi: 10.1128/IAI.59.8.2839-2842.1991 – volume: 85 start-page: 88 year: 2009 ident: B10 article-title: The cytolytic enzymes granyzme A, granzyme B, and perforin: expression patterns, cell distribution, and their relationship to cell maturity and bright CD57 expression publication-title: J. Leukoc. Biol doi: 10.1189/jlb.0208107 – volume: 13 start-page: 304 year: 2017 ident: B43 article-title: Performance of Leishmania PFR1 recombinant antigen in serological diagnosis of asymptomatic canine leishmaniosis by ELISA publication-title: BMC Vet. Res doi: 10.1186/s12917-017-1224-z – volume: 480 start-page: 180 year: 2015 ident: B35 article-title: T cell exhaustion during persistent viral infections publication-title: Virology doi: 10.1016/j.virol.2014.12.033 – volume: 2 start-page: 165 year: 2014 ident: B14 article-title: The role of CD4 and CD8 T cells in human cutaneous Leishmaniasis publication-title: Front. Public Health doi: 10.3389/fpubh.2014.00165 – volume: 90 start-page: 95 year: 1997 ident: B65 article-title: A motility function for the paraflagellar rod of Leishmania parasites revealed by PFR-2 gene knockouts publication-title: Mol. Biochem. Parasitol doi: 10.1016/S0166-6851(97)00149-7 – volume: 9 start-page: 251 year: 2002 ident: B16 article-title: T-cell-mediated immune responses in patients with cutaneous or mucosal leishmaniasis: long-term evaluation after therapy publication-title: Clin. Diagn. Lab. Immunol doi: 10.1128/CDLI.9.2.251-256.2002 – volume: 209 start-page: 290 year: 2014 ident: B29 article-title: CD8 T cell exhaustion in human visceral leishmaniasis publication-title: J. Infect. Dis doi: 10.1093/infdis/jit401 – volume: 63 start-page: 169 year: 1988 ident: B6 article-title: The paraflagellar rod: a structure in search of a function publication-title: Biol. Cell doi: 10.1016/0248-4900(88)90056-1 – volume: 31 start-page: 139 year: 1998 ident: B13 article-title: Immunologic patterns associated with cure in human American cutaneous leishmaniasis publication-title: Braz. J. Med. Biol. Res doi: 10.1590/S0100-879X1998000100019 – volume: 100 start-page: 1112 year: 2006 ident: B19 article-title: Haematogenous dissemination of Leishmania (Viannia) braziliensis in human American tegumentary leishmaniasis publication-title: Trans. R. Soc. Trop. Med. Hyg doi: 10.1016/j.trstmh.2006.02.014 – volume: 5 start-page: e1000431 year: 2009 ident: B34 article-title: B7-H1 blockade increases survival of dysfunctional CD8(+) T cells and confers protection against Leishmania donovani infections publication-title: PLoS Pathog doi: 10.1371/journal.ppat.1000431 – volume: 18 start-page: 1742 year: 2017 ident: B72 article-title: Markers of T cell senescence in humans publication-title: Int. J. Mol. Sci doi: 10.3390/ijms18081742 – volume: 62 start-page: 837 year: 1994 ident: B46 article-title: Increased expression of proinflammatory cytokines in chronic lesions of human cutaneous leishmaniasis publication-title: Infect. Immun doi: 10.1128/IAI.62.3.837-842.1994 – volume: 2 start-page: 845 year: 2002 ident: B62 article-title: The immunology of susceptibility and resistance to Leishmania major in mice publication-title: Nat. Rev. Immunol doi: 10.1038/nri933 – volume: 221 start-page: 879 year: 2016 ident: B11 article-title: PD-1 function in apoptosis of T lymphocytes in canine visceral leishmaniasis publication-title: Immunobiology doi: 10.1016/j.imbio.2016.03.007 – volume: 5 start-page: e1204 year: 2011 ident: B33 article-title: TLR1/2 activation during heterologous prime-boost vaccination (DNA-MVA) enhances CD8+ T Cell responses providing protection against Leishmania (Viannia) publication-title: PLoS Negl. Trop. Dis doi: 10.1371/journal.pntd.0001204 – volume: 309 start-page: 50 year: 2016 ident: B31 article-title: Memory T cells in cutaneous leishmaniasis publication-title: Cell Immunol doi: 10.1016/j.cellimm.2016.07.010 – volume: 61 start-page: 220 year: 1993 ident: B1 article-title: Persistence of virulent Leishmania major in murine cutaneous leishmaniasis: a possible hazard for the host publication-title: Infect. Immun doi: 10.1128/IAI.61.1.220-226.1993 – volume: 83 start-page: 898 year: 2015 ident: B7 article-title: Protective and pathological functions of CD8+ T cells in Leishmania braziliensis infection publication-title: Infect. Immun doi: 10.1128/IAI.02404-14 – volume: 4 start-page: e871 year: 2010 ident: B32 article-title: CD8 cells of patients with diffuse cutaneous leishmaniasis display functional exhaustion: the latter is reversed, in vitro, by TLR2 agonists publication-title: PLoS Negl. Trop. Dis doi: 10.1371/journal.pntd.0000871 – volume: 198 start-page: 3170 year: 2017 ident: B45 article-title: Antiparasitic treatment induces an improved CD8(+) T cell response in chronic chagasic patients publication-title: J. Immunol doi: 10.4049/jimmunol.1602095 – volume: 166 start-page: 4012 year: 2001 ident: B71 article-title: Rapidly fatal leishmaniasis in resistant C57BL/6 mice lacking TNF publication-title: J. Immunol doi: 10.4049/jimmunol.166.6.4012 – volume: 189 start-page: 1018 year: 2004 ident: B47 article-title: Persistence of leishmania parasites in scars after clinical cure of American cutaneous leishmaniasis: is there a sterile cure? publication-title: J. Infect. Dis doi: 10.1086/382135 – volume: 24 start-page: 7046 year: 2006 ident: B50 article-title: The genetic immunization with paraflagellar rod protein-2 fused to the HSP70 confers protection against late Trypanosoma cruzi infection publication-title: Vaccine doi: 10.1016/j.vaccine.2006.07.006 – volume: 200 start-page: 638 year: 2009 ident: B26 article-title: Detection of Leishmania in unaffected mucosal tissues of patients with cutaneous leishmaniasis caused by Leishmania (Viannia) species publication-title: J. Infect. Dis doi: 10.1086/600109 – volume: 185 start-page: 202 year: 2016 ident: B20 article-title: Effector memory CD4(+) T cells differentially express activation associated molecules depending on the duration of American cutaneous leishmaniasis lesions publication-title: Clin. Exp. Immunol doi: 10.1111/cei.12798 – volume: 3 start-page: e512 year: 2009 ident: B27 article-title: Profile of central and effector memory T cells in the progression of chronic human chagas disease publication-title: PLoS Negl. Trop. Dis doi: 10.1371/journal.pntd.0000512 – volume: 198 start-page: 191 year: 2003 ident: B69 article-title: Interleukin 1alpha promotes Th1 differentiation and inhibits disease progression in Leishmania major-susceptible BALB/c mice publication-title: J. Exp. Med doi: 10.1084/jem.20030159 – volume: 9 start-page: 1021 year: 2018 ident: B5 article-title: PD-L1 may mediate T-cell exhaustion in a case of early diffuse leishmaniasis caused by Leishmania (L.) amazonensis publication-title: Front. Immunol doi: 10.3389/fimmu.2018.01021 – volume: 31 start-page: 143 year: 1998 ident: B58 article-title: Cytokine profile and pathology in human leishmaniasis publication-title: Braz. J. Med. Biol. Res doi: 10.1590/S0100-879X1998000100020 – volume: 133 start-page: 1533 year: 2013 ident: B64 article-title: CD8(+) granzyme B(+)-mediated tissue injury vs. CD4(+)IFNgamma(+)-mediated parasite killing in human cutaneous leishmaniasis publication-title: J. Invest. Dermatol doi: 10.1038/jid.2013.4 – volume: 71 start-page: 3165 year: 2003 ident: B48 article-title: Humoral and cellular immune responses to Trypanosoma cruzi-derived paraflagellar rod proteins in patients with Chagas' disease publication-title: Infect. Immun doi: 10.1128/IAI.71.6.3165-3171.2003 – volume: 29 start-page: 757 year: 1991 ident: B41 article-title: Immune reactivity to fractionated Leishmania aethiopica antigens during active human infection publication-title: J. Clin. Microbiol doi: 10.1128/JCM.29.4.757-763.1991 – volume: 29 start-page: 671 year: 2007 ident: B61 article-title: CD8 cytotoxic T cells in cutaneous leishmaniasis publication-title: Parasite Immunol doi: 10.1111/j.1365-3024.2007.00991.x – volume: 42 start-page: 206 year: 1990 ident: B12 article-title: Distribution and etiology of leishmaniasis in Colombia publication-title: Am. J. Trop. Med. Hyg doi: 10.4269/ajtmh.1990.42.206 – volume: 2014 start-page: 636039 year: 2014 ident: B52 article-title: Involvement of different CD4(+) T cell subsets producing granzyme B in the immune response to Leishmania major antigens publication-title: Mediat. Inflamm doi: 10.1155/2014/636039 – volume: 31 start-page: 432 year: 2009 ident: B25 article-title: Recruitment of CD8(+) T cells expressing granzyme A is associated with lesion progression in human cutaneous leishmaniasis publication-title: Parasite Immunol doi: 10.1111/j.1365-3024.2009.01125.x – volume: 195 start-page: 3748 year: 2015 ident: B42 article-title: Inhibitory receptor expression on CD8+ T cells is linked to functional responses against Trypanosoma cruzi Antigens in chronic chagasic patients publication-title: J. Immunol doi: 10.4049/jimmunol.1500459 – volume: 16 start-page: 99 year: 2015 ident: B21 article-title: Cutaneous leishmaniasis: recent developments in diagnosis and management publication-title: Am. J. Clin. Dermatol doi: 10.1007/s40257-015-0114-z – volume: 9 start-page: e0004178 year: 2015 ident: B40 article-title: The immunology of a healing response in cutaneous Leishmaniasis treated with localized heat or systemic antimonial therapy publication-title: PLoS Negl. Trop. Dis doi: 10.1371/journal.pntd.0004178 – volume: 39 start-page: 1700 year: 2009 ident: B4 article-title: CTL quality and the control of human retroviral infections publication-title: Eur. J. Immunol doi: 10.1002/eji.200939451 – volume: 9 start-page: e1003504 year: 2013 ident: B53 article-title: Cytotoxic T cells mediate pathology and metastasis in cutaneous leishmaniasis publication-title: PLoS Pathog doi: 10.1371/journal.ppat.1003504 – volume: 7 start-page: 151 year: 2016 ident: B18 article-title: Cutaneous Leishmaniasis vaccination: a matter of quality publication-title: Front. Immunol doi: 10.3389/fimmu.2016.00151 – volume: 191 start-page: 5542 year: 2013 ident: B24 article-title: Programmed death 1-mediated T cell exhaustion during visceral leishmaniasis impairs phagocyte function publication-title: J. Immunol doi: 10.4049/jimmunol.1301810 – volume: 31 start-page: 423 year: 2009 ident: B67 article-title: Immunopathogenic competences of Leishmania (V.) braziliensis and L. (L.) amazonensis in American cutaneous leishmaniasis publication-title: Parasite Immunol doi: 10.1111/j.1365-3024.2009.01116.x – volume: 52 start-page: 289 year: 2012 ident: B23 article-title: Trypanosoma cruzi paraflagellar rod proteins 2 and 3 contain immunodominant CD8(+) T-cell epitopes that are recognized by cytotoxic T cells from Chagas disease patients publication-title: Mol. Immunol doi: 10.1016/j.molimm.2012.05.021 – volume: 14 start-page: 702 year: 2012 ident: B38 article-title: Phenotyping of circulating CD8(+) T cell subsets in human cutaneous leishmaniasis publication-title: Microbes Infect doi: 10.1016/j.micinf.2012.02.006 – volume: 22 start-page: 745 year: 2004 ident: B63 article-title: Central memory and effector memory T cell subsets: function, generation, and maintenance publication-title: Annu. Rev. Immunol doi: 10.1146/annurev.immunol.22.012703.104702 – volume: 36 start-page: 58 year: 2006 ident: B44 article-title: PD-L1 and PD-L2 have distinct roles in regulating host immunity to cutaneous leishmaniasis publication-title: Eur. J. Immunol doi: 10.1002/eji.200535458 – volume: 28 start-page: 377 year: 2012 ident: B30 article-title: T cell exhaustion in protozoan disease publication-title: Trends Parasitol doi: 10.1016/j.pt.2012.07.001 – ident: B70 |
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Title | Phenotypic and Functional Profiles of Antigen-Specific CD4+ and CD8+ T Cells Associated With Infection Control in Patients With Cutaneous Leishmaniasis |
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