A remarkable feature of the adaptive immune system is the speed at which small numbers of antigen-specific lymphocytes can mediate a successful immune response. Rapid expansion of T and B lymphocyte clones that have receptors specific for a particular antigen is one of the primary means by which a swift response is generated. Although much of this clonal expansion is caused by the division of antigen-specific cells, here we demonstrate an additional mechanism by which the pool of effector T cells against a viral infection can quickly enlarge. Our data show that virus-specific CD8+ cytotoxic T lymphocytes (CTL) can transfer their T cell receptors (TCR) to recipient CTL of an unrelated specificity that, as a consequence, gain the antigen specificity of the donor T cell. This process occurs within minutes via membrane exchange and results in the recipient CTL acquiring the ability to recognize and eliminate cells targeted by the donor TCR, while still retaining the antigen specificity of its own TCR. Such receptor sharing allows rapid, proliferation-independent expansion of virus-specific T cell clones of low frequency and plays a highly significant antiviral role that can protect the host from an otherwise lethal infection.
History
Publication title
National Academy of Sciences of The United States of America. Proceedings
Volume
106
Issue
35
Pagination
14984-9
ISSN
0027-8424
Department/School
Tasmanian School of Medicine
Publisher
Natl Acad Sciences
Place of publication
2101 Constitution Ave Nw, Washington, USA, Dc, 20418
Rights statement
Copyright 2020 the authors
Repository Status
Restricted
Socio-economic Objectives
Prevention of human diseases and conditions; Treatment of human diseases and conditions