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Publication : The limits of protection by "memory" T cells in Ig-/- mice persistently infected with a gamma-herpesvirus.

First Author  Andreansky S Year  2004
Journal  Proc Natl Acad Sci U S A Volume  101
Issue  7 Pages  2017-22
PubMed ID  14764895 Mgi Jnum  J:88442
Mgi Id  MGI:3033278 Doi  10.1073/pnas.0307320101
Citation  Andreansky S, et al. (2004) The limits of protection by 'memory' T cells in Ig-/- mice persistently infected with a gamma-herpesvirus. Proc Natl Acad Sci U S A 101(7):2017-22
abstractText  Can CD4(+) and CD8(+) 'memory' T cells that are generated and maintained in the context of low-level virus persistence protect, in the absence of antibody, against a repeat challenge with the same pathogen? Although immune T cells exert effective, long-term control of a persistent gamma-herpesvirus (gammaHV68) in Ig(-/-) microMT mice, subsequent exposure to a high dose of the same virus leads to further low-level replication in the lung. This lytic phase in the respiratory tract is dealt with effectively by the recall of memory T cells induced by a gammaHV68 recombinant (M3LacZ) that does not express the viral M3 chemokine binding protein. At least for the CD8(+) response, greater numbers of memory T cells confer enhanced protection in the M3LacZ-immune mice. However, neither WT gammaHV68 nor the minimally persistent M3LacZ primes the T cell response to the extent that a WT gammaHV68 challenge fails to establish latency in the microMT mice. Memory CD4(+) and CD8(+) T cells thus act together to limit gammaHV68 infection but are unable to provide absolute protection against a high-dose, homologous challenge.
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