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      The CD8 + T Cell Noncytotoxic Antiviral Responses

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          Abstract

          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.

          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.

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          Most cited references435

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          Avian flu: influenza virus receptors in the human airway.

          Although more than 100 people have been infected by H5N1 influenza A viruses, human-to-human transmission is rare. What are the molecular barriers limiting human-to-human transmission? Here we demonstrate an anatomical difference in the distribution in the human airway of the different binding molecules preferred by the avian and human influenza viruses. The respective molecules are sialic acid linked to galactose by an alpha-2,3 linkage (SAalpha2,3Gal) and by an alpha-2,6 linkage (SAalpha2,6Gal). Our findings may provide a rational explanation for why H5N1 viruses at present rarely infect and spread between humans although they can replicate efficiently in the lungs.
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            T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases.

            Primary T-cell responses in lymph nodes (LNs) require contact-dependent information exchange between T cells and dendritic cells (DCs). Because lymphocytes continually enter and leave normal LNs, the resident lymphocyte pool is composed of non-synchronized cells with different dwell times that display heterogeneous behaviour in mouse LNs in vitro. Here we employ two-photon microscopy in vivo to study antigen-presenting DCs and naive T cells whose dwell time in LNs was synchronized. During the first 8 h after entering from the blood, T cells underwent multiple short encounters with DCs, progressively decreased their motility, and upregulated activation markers. During the subsequent 12 h T cells formed long-lasting stable conjugates with DCs and began to secrete interleukin-2 and interferon-gamma. On the second day, coinciding with the onset of proliferation, T cells resumed their rapid migration and short DC contacts. Thus, T-cell priming by DCs occurs in three successive stages: transient serial encounters during the first activation phase are followed by a second phase of stable contacts culminating in cytokine production, which makes a transition into a third phase of high motility and rapid proliferation.
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              The immunoreceptor TIGIT regulates antitumor and antiviral CD8(+) T cell effector function.

              Tumors constitute highly suppressive microenvironments in which infiltrating T cells are "exhausted" by inhibitory receptors such as PD-1. Here we identify TIGIT as a coinhibitory receptor that critically limits antitumor and other CD8(+) T cell-dependent chronic immune responses. TIGIT is highly expressed on human and murine tumor-infiltrating T cells, and, in models of both cancer and chronic viral infection, antibody coblockade of TIGIT and PD-L1 synergistically and specifically enhanced CD8(+) T cell effector function, resulting in significant tumor and viral clearance, respectively. This effect was abrogated by blockade of TIGIT's complementary costimulatory receptor, CD226, whose dimerization is disrupted upon direct interaction with TIGIT in cis. These results define a key role for TIGIT in inhibiting chronic CD8(+) T cell-dependent responses.
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                Author and article information

                Journal
                Microbiol Mol Biol Rev
                Microbiol Mol Biol Rev
                mmbr
                mmbr
                MMBR
                Microbiology and Molecular Biology Reviews : MMBR
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                1092-2172
                1098-5557
                12 May 2021
                June 2021
                12 May 2021
                : 85
                : 2
                : e00155-20
                Affiliations
                [a ]Division of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, California, USA
                [b ]Versatope Therapeutics Inc., Lowell, Massachusetts, USA
                Author notes
                Address correspondence to Jay A. Levy, jay.levy@ 123456ucsf.edu .

                Citation Morvan MG, Teque FC, Locher CP, Levy JA. 2021. The CD8 + T cell noncytotoxic antiviral responses. Microbiol Mol Biol Rev 85:e00155-20. https://doi.org/10.1128/MMBR.00155-20.

                Author information
                https://orcid.org/0000-0001-5978-6894
                https://orcid.org/0000-0002-7584-3702
                Article
                00155-20
                10.1128/MMBR.00155-20
                8139528
                33980586
                36d5798a-42d2-48cf-bc0f-7ed5bd6be667
                Copyright © 2021 American Society for Microbiology.

                All Rights Reserved.

                This article is made available via the PMC Open Access Subset for unrestricted noncommercial re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                Page count
                Figures: 8, Tables: 7, Equations: 0, References: 434, Pages: 62, Words: 44642
                Categories
                Review
                Custom metadata
                June 2021

                cd8+ t cells,hiv transcription,elite controllers,human immunodeficiency virus,innate immunity,noncytotoxic antiviral activity,soluble antiviral factor

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