Cargando…
In situ detection of Gag-specific CD8(+ )cells in the GI tract of SIV infected Rhesus macaques
BACKGROUND: SIV and HIV predominantly replicate in lymphoid tissue, but the study of virus specific CD8(+ )T cells in intact lymphoid tissue is difficult, as traditional in situ tetramer staining requires fresh tissue. RESULTS: In this report, we demonstrate a novel technique using Qdot 655-conjugat...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834607/ https://www.ncbi.nlm.nih.gov/pubmed/20158906 http://dx.doi.org/10.1186/1742-4690-7-12 |
_version_ | 1782178579045416960 |
---|---|
author | Tjernlund, Annelie Zhu, Jia Laing, Kerry Diem, Kurt McDonald, David Vazquez, Julio Cao, Jianhong Ohlen, Claes McElrath, M Juliana Picker, Louis J Corey, Lawrence |
author_facet | Tjernlund, Annelie Zhu, Jia Laing, Kerry Diem, Kurt McDonald, David Vazquez, Julio Cao, Jianhong Ohlen, Claes McElrath, M Juliana Picker, Louis J Corey, Lawrence |
author_sort | Tjernlund, Annelie |
collection | PubMed |
description | BACKGROUND: SIV and HIV predominantly replicate in lymphoid tissue, but the study of virus specific CD8(+ )T cells in intact lymphoid tissue is difficult, as traditional in situ tetramer staining requires fresh tissue. RESULTS: In this report, we demonstrate a novel technique using Qdot 655-conjugated peptide-MHC multimers to directly visualize SIV specific cells in cryopreserved tissue biopsies from chronically SIVmac239 infected Rhesus macaques. Qdot 655 multimers showed similar sensitivity and specificity to APC-conjugated tetramers by flow cytometry analysis, but yielded ten-fold higher signal intensity when imaged by fluorescence microscopy. Using this technique, we detected CD8(+ )T cells which recognize an immunodominant epitope (Gag CM9) in the spleen, lymph nodes, ileum and colon. In all these tissues, the Gag CM9 positive cells were mainly located in the extra follicular T cell zone. In the ileum and colon, we found Gag CM9 positive cells concentrated in Peyer's patches and solitary lymphoid follicles, a pattern of localization not previously described. CONCLUSIONS: The use of Qdot multimers provide an anatomic and quantitative evaluation of SIV specific CD8(+ )T cell responses in SIV pathogenesis, and may prove useful to studies of SIV specific CD8(+ )T cell responses elicited by vaccines and other immunotherapies in the non-human primate model. |
format | Text |
id | pubmed-2834607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28346072010-03-09 In situ detection of Gag-specific CD8(+ )cells in the GI tract of SIV infected Rhesus macaques Tjernlund, Annelie Zhu, Jia Laing, Kerry Diem, Kurt McDonald, David Vazquez, Julio Cao, Jianhong Ohlen, Claes McElrath, M Juliana Picker, Louis J Corey, Lawrence Retrovirology Research BACKGROUND: SIV and HIV predominantly replicate in lymphoid tissue, but the study of virus specific CD8(+ )T cells in intact lymphoid tissue is difficult, as traditional in situ tetramer staining requires fresh tissue. RESULTS: In this report, we demonstrate a novel technique using Qdot 655-conjugated peptide-MHC multimers to directly visualize SIV specific cells in cryopreserved tissue biopsies from chronically SIVmac239 infected Rhesus macaques. Qdot 655 multimers showed similar sensitivity and specificity to APC-conjugated tetramers by flow cytometry analysis, but yielded ten-fold higher signal intensity when imaged by fluorescence microscopy. Using this technique, we detected CD8(+ )T cells which recognize an immunodominant epitope (Gag CM9) in the spleen, lymph nodes, ileum and colon. In all these tissues, the Gag CM9 positive cells were mainly located in the extra follicular T cell zone. In the ileum and colon, we found Gag CM9 positive cells concentrated in Peyer's patches and solitary lymphoid follicles, a pattern of localization not previously described. CONCLUSIONS: The use of Qdot multimers provide an anatomic and quantitative evaluation of SIV specific CD8(+ )T cell responses in SIV pathogenesis, and may prove useful to studies of SIV specific CD8(+ )T cell responses elicited by vaccines and other immunotherapies in the non-human primate model. BioMed Central 2010-02-16 /pmc/articles/PMC2834607/ /pubmed/20158906 http://dx.doi.org/10.1186/1742-4690-7-12 Text en Copyright ©2010 Tjernlund et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Tjernlund, Annelie Zhu, Jia Laing, Kerry Diem, Kurt McDonald, David Vazquez, Julio Cao, Jianhong Ohlen, Claes McElrath, M Juliana Picker, Louis J Corey, Lawrence In situ detection of Gag-specific CD8(+ )cells in the GI tract of SIV infected Rhesus macaques |
title | In situ detection of Gag-specific CD8(+ )cells in the GI tract of SIV infected Rhesus macaques |
title_full | In situ detection of Gag-specific CD8(+ )cells in the GI tract of SIV infected Rhesus macaques |
title_fullStr | In situ detection of Gag-specific CD8(+ )cells in the GI tract of SIV infected Rhesus macaques |
title_full_unstemmed | In situ detection of Gag-specific CD8(+ )cells in the GI tract of SIV infected Rhesus macaques |
title_short | In situ detection of Gag-specific CD8(+ )cells in the GI tract of SIV infected Rhesus macaques |
title_sort | in situ detection of gag-specific cd8(+ )cells in the gi tract of siv infected rhesus macaques |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834607/ https://www.ncbi.nlm.nih.gov/pubmed/20158906 http://dx.doi.org/10.1186/1742-4690-7-12 |
work_keys_str_mv | AT tjernlundannelie insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT zhujia insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT laingkerry insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT diemkurt insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT mcdonalddavid insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT vazquezjulio insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT caojianhong insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT ohlenclaes insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT mcelrathmjuliana insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT pickerlouisj insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques AT coreylawrence insitudetectionofgagspecificcd8cellsinthegitractofsivinfectedrhesusmacaques |