The third group of the B7-CD28 immune checkpoint family: HHLA2, TMIGD2, B7x, and B7-H3

Murali Janakiram, Urvi A. Shah, Weifeng Liu, Aimin Zhao, Mark P. Schoenberg, Xingxing Zang

Research output: Contribution to journalReview article

53 Scopus citations

Abstract

The B7-CD28 family of ligands and receptors play important roles in T-cell co-stimulation and co-inhibition. Phylogenetically they can be divided into three groups. The recent discovery of the new molecules (B7-H3 [CD276], B7x [B7-H4/B7S1], and HHLA2 [B7H7/B7-H5]/TMIGD2 [IGPR-1/CD28H]) of the group III has expanded therapeutic possibilities for the treatment of human diseases. In this review, we describe the discovery, structure, and function of B7-H3, B7x, HHLA2, and TMIGD2 in immune regulation. We also discuss their roles in important pathological states such as cancers, autoimmune diseases, transplantation, and infection. Various immunotherapeutical approaches are emerging including antagonistic monoclonal antibodies and agonistic fusion proteins to inhibit or potentiate these molecules and pathways in cancers and autoimmune diseases.

Original languageEnglish (US)
Pages (from-to)26-39
Number of pages14
JournalImmunological Reviews
Volume276
Issue number1
DOIs
StatePublished - Mar 1 2017

    Fingerprint

Keywords

  • B7-H3
  • B7x
  • HHLA2
  • TMIGD2
  • immune checkpoint
  • immunotherapy

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

Cite this