The surveillance of viral infections by the unconventional Type I NKT cell

Front Immunol. 2024 Sep 17:15:1472854. doi: 10.3389/fimmu.2024.1472854. eCollection 2024.

Abstract

Type I NKT cells, also known as Invariant Natural Killer T (iNKT) cells, are a subpopulation of unconventional, innate-like T (ILT) cells which can proficiently influence downstream immune effector functions. Type I NKT cells express a semi-invariant αβ T cell receptor (TCR) that recognises lipid-based ligands specifically presented by the non-classical cluster of differentiation (CD1) protein d (CD1d) molecule. Due to their potent immunomodulatory functional capacity, type I NKT cells are being increasingly considered in prophylactic and therapeutic approaches towards various diseases, including as vaccine-adjuvants. As viruses do not encode lipid synthesis, it is surprising that many studies have shown that some viruses can directly impede type I NKT activation through downregulating CD1d expression. Therefore, in order to harness type I NKT cells for potential anti-viral therapeutic uses, it is critical that we fully appreciate how the CD1d-iNKT cell axis interacts with viral immunity. In this review, we examine clinical findings that underpin the importance of type I NKT cell function in viral infections. This review also explores how certain viruses employ immunoevasive mechanisms and directly encode functions to target CD1d expression and type I NKT cell function. Overall, we suggest that the CD1d-iNKT cell axis may hold greater gravity within viral infections than what was previously appreciated.

Keywords: CD1d-iNKT cell axis; type I NKT cell; type I iNKT cell function; unconventional innate-like T cell; viral infections.

Publication types

  • Review

MeSH terms

  • Animals
  • Antigens, CD1d* / immunology
  • Antigens, CD1d* / metabolism
  • Humans
  • Lymphocyte Activation / immunology
  • Natural Killer T-Cells* / immunology
  • Virus Diseases* / immunology

Substances

  • Antigens, CD1d

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.