Interleukin-7-enhanced cytotoxic T lymphocyte activity after viral infection in marrow transplanted mice

A. Abdul-Hai, A. Ben-Yehuda, L. Weiss, G. Friedman, Z. Zakay-Rones, S. Slavin, R. Or*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Lethally irradiated BALB/c mice were reconstituted by syngeneic bone marrow transplantation (BMT), and injected with recombinant interleukin 7 (rIL-7), recombinant interleukin 2 (rIL-2), or saline 10 days post-transplantation. Intranasal infection with A/PR8/34 influenza virus 2 weeks after BMT was associated with the highest survival rate in the rIL-7-treated group. The protective mechanism elicited by rLL-7, as manifested by very low virus titers in the lung, involves T and B cell functions. High hemagglutinin inhibition antibody levels were observed on days 7 and 12 post-challenge in the rIL-7 mice. Moreover, the anti-influenza cytotoxic T lymphocyte activity was induced primarily by rIL-7, leaving the effect of rIL-2 on the same level as that of the control. Thus, rIL-7 promotes both T cell-mediated function and B cell production during the immunodeficient state after BMT. This cytokine may prove a potential immunotherapeutic modality in BMT recipients.

Original languageEnglish
Pages (from-to)539-543
Number of pages5
JournalBone Marrow Transplantation
Volume19
Issue number6
DOIs
StatePublished - 2 Mar 1997

Keywords

  • Bone marrow transplantation
  • Interleukin 7
  • T lymphocytes

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