PRIMARY HUMAN IMMUNE-RESPONSE TO NEISSERIA-MENINGITIDIS SEROGROUP-C IN INTERLEUKIN-12-TREATED SEVERE COMBINED IMMUNODEFICIENT MICE ENGRAFTED WITH HUMAN PERIPHERAL-BLOOD LYMPHOCYTES
Maj. Westerink et al., PRIMARY HUMAN IMMUNE-RESPONSE TO NEISSERIA-MENINGITIDIS SEROGROUP-C IN INTERLEUKIN-12-TREATED SEVERE COMBINED IMMUNODEFICIENT MICE ENGRAFTED WITH HUMAN PERIPHERAL-BLOOD LYMPHOCYTES, The Journal of infectious diseases, 175(1), 1997, pp. 84-90
Lack of primary immune response in severe combined immunodeficient (SC
ID) mice engrafted with human peripheral blood lymphocytes (hu-PBL) ha
s limited the applicability of this model. Use of human cytokines, in
particular interleukin (IL)-12, was studied in the hu-PBL-SCID model.
SCID mice were treated with IL-12 and reconstituted with hu-PBL in T r
eplacement factor. The hu-PBL-SCID mice were immunized with serogroup
C meningococcal polysaccharide (MCPS). The MCPS-specific antibody resp
onse was determined by ELISA. Thirteen of the 15 immunized, IL-12-trea
ted hu-PBL-SCID mice demonstrated a primary human antibody response to
MCPS ranging from 0.25 to 3.3 mu g/mL, while no MCPS-specific antibod
y response was detectable in the 18 controls. Expression of cross-reac
tive idiotypic markers found on human anti-MCPS antibodies in the immu
nized hu-PBL-SCID mice was similar to that observed in immunized volun
teers.