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Front Immunol. 2017 Mar 27;8:338. doi: 10.3389/fimmu.2017.00338. eCollection 2017.

Negative Checkpoint Regulatory Molecule 2B4 (CD244) Upregulation Is Associated with Invariant Natural Killer T Cell Alterations and Human Immunodeficiency Virus Disease Progression.

Frontiers in immunology

Fareed Ahmad, Esaki M Shankar, Yean K Yong, Hong Y Tan, Gerrit Ahrenstorf, Roland Jacobs, Marie Larsson, Reinhold E Schmidt, Adeeba Kamarulzaman, Abdul W Ansari

Affiliations

  1. Department of Clinical Immunology and Rheumatology, Hannover Medical School , Hannover , Germany.
  2. Centre of Excellence for Research in AIDS (CERiA), University of Malaya, Kuala Lumpur, Malaysia; Department of Medical Microbiology, University of Malaya, Kuala Lumpur, Malaysia; Division of Infection Biology, Department of Life Sciences, School of Basic & Applied Sciences, Central University of Tamil Nadu (CUTN), Thiruvarur, India.
  3. Centre of Excellence for Research in AIDS (CERiA), University of Malaya , Kuala Lumpur , Malaysia.
  4. Division of Molecular Virology, Department of Clinical and Experimental Medicine, Linkoping University , Linkoping , Sweden.
  5. Centre of Excellence for Research in AIDS (CERiA), University of Malaya, Kuala Lumpur, Malaysia; Department of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

PMID: 28396665 PMCID: PMC5366318 DOI: 10.3389/fimmu.2017.00338

Abstract

The CD1d-restricted invariant natural killer T (iNKT) cells are implicated in innate immune responses against human immunodeficiency virus (HIV). However, the determinants of cellular dysfunction across the iNKT cells subsets are seldom defined in HIV disease. Herein, we provide evidence for the involvement of the negative checkpoint regulator (NCR) 2B4 in iNKT cell alteration in a well-defined cohort of HIV-seropositive anti-retroviral therapy (ART) naïve, ART-treated, and elite controllers (ECs). We report on exaggerated 2B4 expression on iNKT cells of HIV-infected treatment-naïve individuals. In sharp contrast to CD4

Keywords: 2B4; CD4; IFN-γ; human immunodeficiency virus; inhibitory; invariant natural killer T cells

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