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The self-nonself concept as a basis for immune complex to replace "autoimmune diseases"
Summary
A 1951 case study reveals that induced anti-P1 IgG antibodies may fight gastric adenocarcinoma by targeting galactose on cancer cells. This immune mechanism might also explain abortions and autoimmune diseases linked to foreign antigens.
Area of Science:
- Immunology
- Oncology
- Genetics
Background:
- Gastric adenocarcinoma presents a unique case for understanding immune responses.
- The self-non-self concept is crucial in distinguishing host tissues from foreign antigens like glycolipid (GL) antigens and Forssman (Fs) antigen.
- Autoimmune diseases share similarities with cancer in immune complex (IC) deposition and tissue damage.
Observation:
- A 1951 patient with gastric adenocarcinoma survived 22 years post-surgery without metastasis after induced anti-P1 IgG antibodies.
- Anti-P1 antibodies likely target the galactose sugar on cancer cells, initiating a cytotoxic cellular immune response.
- Reduced anti-Forssman (Fs) antibodies were observed in cancer patients and the elderly, suggesting age-related immune changes.
Findings:
- Induced anti-P1 IgG antibodies demonstrated a two-stage cytotoxic effect against gastric adenocarcinoma cells.
- The presence of GL and Fs antigens in cancer and autoimmune conditions supports the self-non-self hypothesis.
- Normal serum contains antibodies against missing GL antigens, with anti-Fs prevalence decreasing with age.
Implications:
- The anti-P1 immune mechanism may be relevant for treating gastric cancer and understanding pregnancy loss.
- Understanding immune responses to foreign antigens is key to addressing autoimmune diseases like rheumatoid arthritis and lupus.
- Plasma exchange therapy is suggested to replenish IgG antibodies and complement in autoimmune conditions.