scholarly journals The CD8+ T Cell Noncytotoxic Antiviral Responses

2021 ◽  
Vol 85 (2) ◽  
Author(s):  
Maelig G. Morvan ◽  
Fernando C. Teque ◽  
Christopher P. Locher ◽  
Jay A. Levy

SUMMARY The CD8+ T cell noncytotoxic antiviral response (CNAR) was discovered during studies of asymptomatic HIV-infected subjects more than 30 years ago. In contrast to CD8+ T cell cytotoxic lymphocyte (CTL) activity, CNAR suppresses HIV replication without target cell killing. This activity has characteristics of innate immunity: it acts on all retroviruses and thus is neither epitope specific nor HLA restricted. The HIV-associated CNAR does not affect other virus families. It is mediated, at least in part, by a CD8+ T cell antiviral factor (CAF) that blocks HIV transcription. A variety of assays used to measure CNAR/CAF and the effects on other retrovirus infections are described. Notably, CD8+ T cell noncytotoxic antiviral responses have now been observed with other virus families but are mediated by different cytokines. Characterizing the protein structure of CAF has been challenging despite many biologic, immunologic, and molecular studies. It represents a low-abundance protein that may be identified by future next-generation sequencing approaches. Since CNAR/CAF is a natural noncytotoxic activity, it could provide promising strategies for HIV/AIDS therapy, cure, and prevention.

Cell Reports ◽  
2021 ◽  
Vol 35 (6) ◽  
pp. 109103
Author(s):  
Hongbing Yang ◽  
Anuska Llano ◽  
Samandhy Cedeño ◽  
Annette von Delft ◽  
Angelica Corcuera ◽  
...  

Author(s):  
Michael L. Greenberg ◽  
Simon F. Lacey ◽  
Chin-Ho Chen ◽  
Dani P. Bolognesi ◽  
Kent J. Weinhold
Keyword(s):  
T Cell ◽  

1997 ◽  
Vol 13 (1) ◽  
pp. 63-69 ◽  
Author(s):  
ANDREA RUBBERT ◽  
DREW WEISSMAN ◽  
CHRISTOPHE COMBADIERE ◽  
KRISTEN A. PETTRONE ◽  
JAMES A. DAUCHER ◽  
...  

2020 ◽  
Author(s):  
Hongbing Yang ◽  
Anuska Llano ◽  
Samandhy Cedeño ◽  
Annette von Delft ◽  
Angelica Corcuera ◽  
...  

Blood ◽  
2012 ◽  
Vol 119 (20) ◽  
pp. 4645-4655 ◽  
Author(s):  
Daniel Mendoza ◽  
Sarah A. Johnson ◽  
Bennett A. Peterson ◽  
Ven Natarajan ◽  
Maria Salgado ◽  
...  

Abstract True long-term nonprogressors (LTNPs)/elite controllers (ECs) maintain durable control over HIV replication without antiretroviral therapy. Herein we describe 4 unique persons who were distinct from conventional LTNPs/ECs in that they had extraordinarily low HIV burdens and comparatively weak immune responses. As a group, typical LTNPs/ECs have unequivocally reactive HIV-1 Western blots, viral loads below the lower threshold of clinical assays, low levels of persistent viral reservoirs, an over-representation of protective HLA alleles, and robust HIV-specific CD8+ T-cell responses. The 4 unique cases were distinguished from typical LTNPs/ECs based on weakly reactive Western blots, undetectable plasma viremia by a single copy assay, extremely low to undetectable HIV DNA levels, and difficult to isolate replication-competent virus. All 4 had at least one protective HLA allele and CD8+ T-cell responses that were disproportionately high for the low antigen levels but comparatively lower than those of typical LTNPs/ECs. These unique persons exhibit extraordinary suppression over HIV replication, therefore, higher-level control than has been demonstrated in previous studies of LTNPs/ECs. Additional insight into the full spectrum of immune-mediated suppression over HIV replication may enhance our understanding of the associated mechanisms, which should inform the design of efficacious HIV vaccines and immunotherapies.


Blood ◽  
2011 ◽  
Vol 118 (8) ◽  
pp. 2138-2149 ◽  
Author(s):  
Maria Candela Iglesias ◽  
Jorge R. Almeida ◽  
Solène Fastenackels ◽  
David J. van Bockel ◽  
Masao Hashimoto ◽  
...  

AbstractMapping the precise determinants of T-cell efficacy against viruses in humans is a public health priority with crucial implications for vaccine design. To inform this effort, we performed a comprehensive analysis of the effective CD8+ T-cell clonotypes that constitute responses specific for the HIV p24 Gag-derived KK10 epitope (KRWIILGLNK; residues 263-272) restricted by HLA-B*2705, which are known to confer superior control of viral replication in HIV-infected individuals. Particular KK10-specific CD8+ T-cell clonotypes, characterized by TRBV4-3/TRBJ1-3 gene rearrangements, were found to be preferentially selected in vivo and shared between individuals. These “public” clonotypes exhibit high levels of TCR avidity and Ag sensitivity, which impart functional advantages and enable effective suppression of HIV replication. The early L268M mutation at position 6 of the KK10 epitope enables the virus to avoid recognition by these highly effective CD8+ T-cell clonotypes. However, alternative clonotypes with variant reactivity provide flexibility within the overall KK10-specific response. These findings provide refined mechanistic insights into the workings of an effective CD8+ T-cell response against HIV.


2011 ◽  
Vol 83 (3) ◽  
pp. 557-557
Author(s):  
Ben Z. Katz ◽  
Babak Salimi ◽  
Samantha L. Gadd ◽  
Chiang-Ching Huang ◽  
William J. Kabat ◽  
...  

1991 ◽  
Vol 7 (9) ◽  
pp. 773-780 ◽  
Author(s):  
FLORENCE BETTENS ◽  
CHRISTIANE E. PICHLER ◽  
BRIGITTE HERRMANN ◽  
ALAIN L. DE WECK ◽  
WERNER J. PICHLER

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