T-cell receptor (TCR)/CD3 is involved in sulfated polymannuroguluronate (SPMG)-induced T lymphocyte activation.

Sulfated polymannuroguluronate (SPMG) has entered the Phase II clinical trial as the first anti-acquired immune deficiency syndrome (AIDS) drug candidate in China. Proliferation assays showed that SPMG was effective at enhancing the proliferative response of T lymphocytes either with or without concanavalin A (ConA) stimulation. Flow cytometry (FCM) and fluorescence microscope examination revealed the significant binding of SPMG to T lymphocytes. The significant engagement of SPMG with TCR/CD3 complex was verified by competitive inhibition assay and one of the SPMG binding proteins purified by affinity chromatography from thymocyte membrane preparations was further confirmed to be CD3 component of TCR/CD3 complex via Western blotting analysis. In addition, SPMG was demonstrated to dramatically interact with ConA in a multivalent manner by surface plasmon resonance (SPR) assay. Notably, the concomitant presence of ConA and SPMG facilitated each other's binding to T cells. Together, the simultaneous interactions of SPMG with TCR/CD3 and with ConA can be highly proposed to facilitate the cross-linking of these molecules, and thus favoring costimulatory signaling, which serves to well explain the immunopotentiation and anti-human immunodeficiency virus (HIV) activities of SPMG.
AuthorsBenchun Miao, Jing Li, Xueyan Fu, Jian Ding, Meiyu Geng
JournalInternational immunopharmacology (Int Immunopharmacol) Vol. 5 Issue 7-8 Pg. 1171-82 (Jul 2005) ISSN: 1567-5769 [Print] Netherlands
PMID15914322 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-HIV Agents
  • Antigens, CD3
  • Polysaccharides
  • Receptors, Antigen, T-Cell
  • sulfated polymannuroguluronate
  • Concanavalin A
  • Animals
  • Anti-HIV Agents (pharmacology)
  • Antigens, CD3 (physiology)
  • Concanavalin A (pharmacology)
  • Lymphocyte Activation (drug effects)
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Polysaccharides (pharmacology)
  • Receptors, Antigen, T-Cell (physiology)
  • T-Lymphocytes (immunology)

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