Why the study?
Does enteral human serum immunoglobulin reduce the intensity of infection or mortality in scid mice infected with Cryptosporidium parvum?
Does enteral human serum immunoglobulin reduce the intensity of infection or mortality in scid mice infected with Cryptosporidium parvum?
Human serum immunoglobulin may be beneficial prophylactically but cannot eradicate established cryptosporidiosis in immunodeficient mice.
Answers are grounded in this paper and cite their sources.
HSIG prophylaxis merits exploration in at-risk populations; leaves open any therapeutic benefit in established cryptosporidiosis.
The anti-cryptosporidial immunoglobulin G antibodies in two commercially available human serum immunoglobulin (HSIG) products were quantified and characterized. The mean level of Cryptosporidium parvum-specific immunoglobulin G in HSIG was eightfold higher than the antibody level found in the sera of three immunocompetent individuals convalescing from cryptosporidiosis. However, HSIG products displayed no reactivity to cryptosporidial antigens in immunoblot analyses, while convalescent-phase sera demonstrated characteristic banding patterns. When HSIG was given to newborn severe combined immunodeficiency (scid) mice before and shortly after experimental infection, a decreased intensity of infection was observed in the intestines of the mice compared with that of control mice. However, there was no difference in mortality or histopathologic findings in the intestines of HSIG-treated and control mice when treatment was not started until 22 days of age. These results indicate that HSIG may be beneficial when given prophylactically; however, HSIG cannot eradicate cryptosporidia from mucosal surfaces in an established infection.
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Kuhls et al. (1995) studied this question.
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