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  4. Antiviral CD8⁺ T Cells Restricted by Human Leukocyte Antigen Class II Exist during Natural HIV Infection and Exhibit Clonal Expansion

Antiviral CD8⁺ T Cells Restricted by Human Leukocyte Antigen Class II Exist during Natural HIV Infection and Exhibit Clonal Expansion

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Author(s)
Ranasinghe, Srinika
•
Lamothe, Pedro A.
•
Soghoian, Damien Z.
•
Cole, Michael B.
•
Yosef, Nir
•
Jones, R. Brad
•
Donaghey, Faith
•
Nwonu, Chioma
•
Jani, Priya
•
Clayton, Gina M.
more
Date Issued
October 2016
Journal
Immunity
Publisher
Elsevier
Citation
Ranasinghe, Srinika et al. “Antiviral CD8⁺ T Cells Restricted by Human Leukocyte Antigen Class II Exist During Natural HIV Infection and Exhibit Clonal Expansion.” Immunity 45, 4 (October 2016): 917–930 © 2016 The Author(s)
Version
Final published version
Abstract
CD8⁺ T cell recognition of virus-infected cells is characteristically restricted by major histocompatibility complex (MHC) class I, although rare examples of MHC class II restriction have been reported in Cd4-deficient mice and a macaque SIV vaccine trial using a recombinant cytomegalovirus vector. Here, we demonstrate the presence of human leukocyte antigen (HLA) class II-restricted CD8⁺ T cell responses with antiviral properties in a small subset of HIV-infected individuals. In these individuals, T cell receptor β (TCRβ) analysis revealed that class II-restricted CD8⁺ T cells underwent clonal expansion and mediated killing of HIV-infected cells. In one case, these cells comprised 12% of circulating CD8⁺ T cells, and TCRα analysis revealed two distinct co-expressed TCRα chains, with only one contributing to binding of the class II HLA-peptide complex. These data indicate that class II-restricted CD8⁺ T cell responses can exist in a chronic human viral infection, and may contribute to immune control. Keywords: HIV; TCR; CD8⁺ T cells; vaccines; HLA;MHC class II
MIT Department
Institute for Medical Engineering and Science
Terms of Use
Creative Commons Attribution 4.0 International License
http://creativecommons.org/licenses/by/4.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/113556
DOI of Published Version
https://doi.org/10.1016/J.IMMUNI.2016.09.015
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