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Antibody-dependent cellular cytotoxicity in poikilotherms
Developmental and Comparative Immunology
|October 1, 1977
Summary
Amphibian and reptile spleen cells can lyse antibody-coated target cells without complement, mimicking antibody-dependent cellular cytotoxicity (ADCC) found in mammals and birds.
Area of Science:
- Comparative immunology
- Cellular cytotoxicity
- Vertebrate immunology
Background:
- Antibody-dependent cellular cytotoxicity (ADCC) is a key immune mechanism in mammals and birds, mediated by K cells.
- The presence and function of similar cytotoxic mechanisms in other vertebrate classes, like amphibians and reptiles, are less understood.
Purpose of the Study:
- To investigate the cytotoxic capabilities of spleen cells from amphibians (Xenopus laevis, Ambystoma mexicanum) and a reptile (Lacerta viridis).
- To determine if these cells can mediate antibody-dependent lysis in the absence of complement.
- To explore the phylogenetic implications of observed cytotoxic phenomena.
Main Methods:
- Chicken red blood cells were labeled with 51Cr-chromate and treated with rabbit anti-chicken red blood cell serum.
- Spleen cells from Xenopus laevis, Ambystoma mexicanum, and Lacerta viridis were incubated with the antibody-coated target cells.
- Cytolysis was quantified by measuring the release of 51Cr in vitro, without the addition of exogenous complement.
Main Results:
- Spleen cells from Xenopus laevis, Ambystoma mexicanum, and Lacerta viridis effectively lysed antibody-coated chicken red blood cells.
- This lysis occurred in the absence of complement, indicating a complement-independent mechanism.
- Optimal conditions for lysis mediated by Xenopus spleen cells were determined.
Conclusions:
- The study demonstrates a functional homologue of antibody-dependent cellular cytotoxicity (ADCC) in amphibians and reptiles.
- This finding suggests that ADCC-like mechanisms may be conserved across a broad range of vertebrate species.
- The results contribute to understanding the evolutionary history of cellular immune responses.