Cytomegalovirus (CMV) Epitope-Specific CD4 + T Cells Are Inflated in HIV + CMV + Subjects
Select CMV epitopes drive life-long CD8 T cell memory inflation, but the extent of CD4 memory inflation is poorly studied. CD4 T cells specific for human CMV (HCMV) are elevated in HIV HCMV subjects. To determine whether HCMV epitope-specific CD4 T cell memory inflation occurs during HIV infection,...
Saved in:
Published in | The Journal of immunology (1950) Vol. 199; no. 9; pp. 3187 - 3201 |
---|---|
Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Association of Immunologists
01.11.2017
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Select CMV epitopes drive life-long CD8
T cell memory inflation, but the extent of CD4 memory inflation is poorly studied. CD4
T cells specific for human CMV (HCMV) are elevated in HIV
HCMV
subjects. To determine whether HCMV epitope-specific CD4
T cell memory inflation occurs during HIV infection, we used HLA-DR7 (DRB1*07:01) tetramers loaded with the glycoprotein B DYSNTHSTRYV (DYS) epitope to characterize circulating CD4
T cells in coinfected HLA-DR7
long-term nonprogressor HIV subjects with undetectable HCMV plasma viremia. DYS-specific CD4
T cells were inflated among these HIV
subjects compared with those from an HIV
HCMV
HLA-DR7
cohort or with HLA-DR7-restricted CD4
T cells from the HIV-coinfected cohort that were specific for epitopes of HCMV phosphoprotein-65, tetanus toxoid precursor, EBV nuclear Ag 2, or HIV gag protein. Inflated DYS-specific CD4
T cells consisted of effector memory or effector memory-RA
subsets with restricted TCRβ usage and nearly monoclonal CDR3 containing novel conserved amino acids. Expression of this near-monoclonal TCR in a Jurkat cell-transfection system validated fine DYS specificity. Inflated cells were polyfunctional, not senescent, and displayed high ex vivo levels of granzyme B, CX
CR1, CD38, or HLA-DR but less often coexpressed CD38
and HLA-DR
The inflation mechanism did not involve apoptosis suppression, increased proliferation, or HIV gag cross-reactivity. Instead, the findings suggest that intermittent or chronic expression of epitopes, such as DYS, drive inflation of activated CD4
T cells that home to endothelial cells and have the potential to mediate cytotoxicity and vascular disease. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-1767 1550-6606 |
DOI: | 10.4049/jimmunol.1700851 |