The radiation‐attenuated schistosome vaccine induces high levels of protective immunity in the absence of B cells

• Published in: Immunology Vol. 96; no. 1; pp. 22 - 28
• Main Authors: Anderson, S, Coulson, P S, Ljubojevic, S, Mountford, A P, Wilson, R A
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science Ltd 01.01.1999; Wiley Subscription Services, Inc; Blackwell Science Inc
• Subjects: AIDS/HIV; Animals; B-Lymphocytes; Immunization Schedule; Interferon-gamma - metabolism; Lung - immunology; Lymph Nodes - immunology; Mice; Mice, Inbred C57BL; Mice, Mutant Strains - immunology; Original; Schistosomiasis mansoni - immunology; Skin; T-Lymphocytes, Helper-Inducer - immunology; Th1 Cells - immunology; Th2 Cells - immunology; Vaccines, Attenuated - administration & dosage
• DOI: 10.1046/j.1365-2567.1999.00661.x
• ISSN: 0019-2805

Radiation‐attenuated cercariae of Schistosoma mansoni elicit consistently high levels of protective immunity in mice. The cell‐mediated pulmonary effector mechanisms have been well characterized but the role of B cells and antibodies remains ill defined. We have compared the immune responses of B‐cell‐deficient (μMT) mice and their wild‐type (WT) counterparts following exposure to the attenuated vaccine. Both groups mounted a T helper type 1 (Th1)‐biased response in the skin‐draining lymph nodes after vaccination. Interferon‐γ was the dominant cytokine secreted by airway leucocytes after challenge in both μMT and WT mice, but there was a somewhat greater Th2 component in the former animals. The cellular infiltrates observed in the airways, and the pulmonary effector foci, were of similar composition in the two groups although some large foci were present in the μMT mice. There was a marked dichotomy in the protection induced in μMT animals by a single vaccination, with two‐thirds showing levels similar to their WT counterparts, demonstrating that cell‐mediated mechanisms alone can provide adequate protection. The remaining μMT mice had a mean worm burden identical to that of their challenge controls. A possible explanation is that a proportion of the μMT animals have a genetic defect closely associated with the μ‐heavy‐chain locus on chromosome 12, which affects their ability to mount a protective cell‐mediated response. Three vaccinations enhanced the immunity of WT animals, most likely by augmenting antibody‐mediated mechanisms. In contrast, no enhancement was seen in μMT mice, suggesting that the cell‐mediated response is not boosted by multiple exposures to attenuated larvae.