A spontaneously arising pancreatic tumor does not promote the differentiation of naive CD8+ T lymphocytes into effector CTL

J Immunol. 2004 Jun 1;172(11):6558-67. doi: 10.4049/jimmunol.172.11.6558.

Abstract

In this report, we address whether a growing tumor provides sufficient inflammatory signals to promote activation, clonal expansion, and acquisition of effector functions by naive tumor-specific CD8(+) T lymphocytes. CD8(+) T lymphocytes obtained from hemagglutinin (HA)-specific clone 4 TCR-transgenic mice were injected into recipient mice that spontaneously develop pancreatic tumors expressing HA as a tumor-associated Ag (RIP-Tag2-HA mice). When 3 x 10(6) clone 4 CD8(+) T cells were transferred into tumor-bearing mice, the cells became activated in the pancreatic lymph nodes where they proliferated and acquired effector functions such as cytolytic activity and IFN-gamma production. Surprisingly, reducing the number of adoptively transferred CD8(+) T cells led to a parallel reduction in the proportion of the activated cells that exhibited effector functions, suggesting that CTL differentiation was induced by the large numbers of activated CD8(+) T cells and not the tumor environment. Provision of tumor-specific CD4(+) helper cells provided the signals required to promote both the development of CTL effector functions and increased clonal expansion, resulting in tumor eradication. Considering that only small numbers of tumor-specific CD8(+) T cells would be present in a conventional T cell repertoire, these data suggest that tumor growth alone may not provide the inflammatory signals necessary to support the development of CD8(+) T cell effector functions.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adoptive Transfer
  • Animals
  • Antigens, Polyomavirus Transforming / genetics
  • CD4-Positive T-Lymphocytes / physiology
  • CD8-Positive T-Lymphocytes / cytology*
  • Cell Differentiation*
  • Cell Line
  • Hemagglutinin Glycoproteins, Influenza Virus / genetics
  • Insulin / genetics
  • Mice
  • Mice, Inbred C57BL
  • Pancreatic Neoplasms / immunology*
  • Promoter Regions, Genetic
  • Rats
  • Receptors, Antigen, T-Cell / physiology
  • T-Lymphocytes, Cytotoxic / cytology*

Substances

  • Antigens, Polyomavirus Transforming
  • Hemagglutinin Glycoproteins, Influenza Virus
  • Insulin
  • Receptors, Antigen, T-Cell