Restricted activity of serum blocking factors related to a common tumour antigen in mice

Oncology
|January 1, 1983
PubMed

Insights

Mice immune cells responded to a synthetic myelin peptide, but tumor-bearing mice developed blocking factors that inhibited this response. These blocking factors were strain-specific, highlighting genetic compatibility in immune interactions.

Area of Science:

  • Immunology
  • Neuroscience
  • Oncology

Background:

  • Cellular immune reactivity is crucial for tumor surveillance.
  • The synthetic encephalitogenic peptide of human myelin basic protein is a known T-cell antigen.
  • Tumor-induced immunosuppression can impair anti-tumor immunity.

Purpose of the Study:

  • To investigate cellular immune reactivity to a myelin basic protein peptide in different mouse strains with transplanted tumors.
  • To identify and characterize blocking factors in tumor-bearing mice that may inhibit immune responses.

Main Methods:

  • Leukocyte adherence inhibition (LAI) assay was used to assess cellular immune reactivity.
  • Four inbred mouse strains (CBA, Balb/c, C57Bl/6, DBA/2) were used.
  • Transplanted tumors included methylcholanthrene-induced sarcomas, B16 melanoma, and P-815 mastocytoma.

Main Results:

  • All tested mouse strains showed reactivity to the myelin peptide at an optimal concentration.
  • Normal and pregnant mice did not exhibit reactivity.
  • Serum from tumor-bearing mice, collected 10+ days post-transplantation, blocked LAI.
  • Blocking factors were cross-reactive between different tumors but only within the same mouse strain.

Conclusions:

  • Tumor transplantation induces immunosuppressive factors that interfere with cellular immune responses.
  • Genetic compatibility between reactive cells and blocking factors is essential for cross-reactivity.
  • These findings have implications for understanding tumor immunology and developing immunotherapies.

Related Concept Videos