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Adoptive suppression of granuloma formation
The Journal of Experimental Medicine
|March 1, 1976
Summary
Cellular immunity, not serum, suppresses granuloma formation in chronic Schistosomiasis mansoni infections. Spleen and lymph node cells from infected mice reduce granuloma size in recipients, with repeated transfers being most effective.
Area of Science:
- Immunology
- Parasitology
- Pathology
Background:
- Granulomas are key to controlling Schistosoma mansoni infection but can cause pathology.
- Granuloma size decreases with chronic infection duration.
Purpose of the Study:
- To investigate the mechanisms behind reduced granuloma size in chronic Schistosomiasis mansoni.
- To determine if serum or cellular components from chronically infected mice mediate this suppression.
Main Methods:
- Passive serum transfer from chronically infected mice to acutely infected recipients.
- Passive cellular transfer (spleen and lymph node cells) from chronically infected mice to acutely infected recipients.
- Assessment of hepatic granuloma size in recipient mice.
Main Results:
- Serum transfer did not alter granuloma size.
- Spleen and lymph node cells from chronically infected mice significantly suppressed granuloma formation.
- Spleen cells from early-infected mice showed some suppressive capacity.
- Sequential cell transfers enhanced suppression.
Conclusions:
- Cellular immunity, mediated by spleen and lymph node cells, is responsible for granuloma size reduction in chronic S. mansoni infection.
- The suppressive capacity of these cells increases with infection chronicity.
- Repeated administration of immune cells may be a therapeutic strategy.

