The CD8+ T Cell Noncytotoxic Antiviral Responses.
Maelig G MorvanFernando C TequeChristopher P LocherJay A LevyPublished in: Microbiology and molecular biology reviews : MMBR (2021)
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.
Keyphrases
- antiretroviral therapy
- hiv aids
- hiv infected
- hiv positive
- human immunodeficiency virus
- rheumatoid arthritis
- hepatitis c virus
- amino acid
- hiv testing
- single cell
- men who have sex with men
- magnetic resonance
- small molecule
- case control
- stem cells
- binding protein
- dna methylation
- mesenchymal stem cells
- transcription factor
- magnetic resonance imaging