IGG ANTIBODY TO PNEUMOCOCCAL CAPSULAR POLYSACCHARIDE IN HUMAN IMMUNODEFICIENCY VIRUS-INFECTED SUBJECTS - PERSISTENCE OF ANTIBODY IN RESPONDERS, REVACCINATION IN NONRESPONDERS, AND RELATIONSHIP OF IMMUNOGLOBULIN ALLOTYPE TO RESPONSE
Mc. Rodriguezbarradas et al., IGG ANTIBODY TO PNEUMOCOCCAL CAPSULAR POLYSACCHARIDE IN HUMAN IMMUNODEFICIENCY VIRUS-INFECTED SUBJECTS - PERSISTENCE OF ANTIBODY IN RESPONDERS, REVACCINATION IN NONRESPONDERS, AND RELATIONSHIP OF IMMUNOGLOBULIN ALLOTYPE TO RESPONSE, The Journal of infectious diseases, 173(6), 1996, pp. 1347-1353
Human immunodeficiency virus (HIV)-infected persons are less likely th
an are noninfected persons to respond to vaccination with pneumococcal
polysaccharides (PPS). Among those who respond, however, similar IgG
levels may be achieved. HIV-infected men immunized with pneumococcal v
accine were classified as high- or low-level responders (IgG greater t
han or equal to 1 mu g/mL for greater than or equal to 3 of 5 PPS [hig
h] or for less than or equal to 1 PPS [low]). One and 2 years after im
munization, geometric mean IgG levels and the percentages of subjects
with IgG levels greater than or equal to 1 mu g/mL were similar for HI
V-infected and for healthy high-level responders (controls) for all PP
S except for serotype 8. Among HIV-infected low-level responders, reva
ccination with a double dose of pneumococcal vaccine did not stimulate
IgG responses. Responsiveness of HIV-infected white patients was sign
ificantly associated with the Km(1)-negative allotype. These findings
support current general recommended guidelines for administering pneum
ococcal vaccine to HIV-infected persons. Nonresponders will not benefi
t from revaccination.