Time course of antibody response to tetanus toxoid and pneumococcal capsular polysaccharides in patients infected with HIV

Citation
E. Talesnik et al., Time course of antibody response to tetanus toxoid and pneumococcal capsular polysaccharides in patients infected with HIV, J ACQ IMM D, 19(5), 1998, pp. 471-477
Citations number
38
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY
ISSN journal
10779450 → ACNP
Volume
19
Issue
5
Year of publication
1998
Pages
471 - 477
Database
ISI
SICI code
1077-9450(199812)19:5<471:TCOART>2.0.ZU;2-G
Abstract
The temporal course of the humoral immune response to T-cell-dependent and T-cell-independent type 2 antigens was evaluated in HIV-infected patients. In all, 26 seropositive patients were vaccinated with tetanus toroid and 23 -valent pneumococcal vaccines; total IgG and IgG1 antibodies to tetanus tor oid (Ttox) and total IgG and IgG2 antibodies against 23 Streptococcus pneum oniae capsular antigens (PPS) were measured at baseline, 2 months, and 12 m onths after vaccination. For the Ttox, baseline levels of IgG1 (Ttox-IgG1) increased from 11.0 to 19.5 mg/L at 2 months postimmunization. Overall only 6 patients (23%) showed a significant response. At 12 months postvaccinati on, Ttox-IgG and T-tox-IgG1 were significantly lower than baseline levels ( Ttox IgG basal; 11.0 mg/L, 12 months; 0.8 mg/L, Ttox IgG1 baseline; 13.1 mg /L, Ttox IgG1 12 months; 2.4 mg/L) and in 10 patients, antibodies that fell below protective levels (0.6 mg/L). In contrast with PPS, a significant re sponse was observed at 2 and 12 months (PPS-IgG basal; 35.9 U/ml, 2 months; 151.4 U/ml, 12 months; 59.7 U/ml; PPS-IgG2 baseline 20.3 U/ml, 2 months; 1 13.2 U/ml, 12 months; 51..9 U/ml). Overall, 19 patients (76%) showed an imm une response to pneumococcal polysaccharides antigens. Immunization with th e Ttox T-cell-dependent antigen fails to elicit a significant immune respon se and may induce inhibition of antibody production in HIV-infected patient s. In contrast, immunization with a T-cell-independent type 2 antigen can c ause the pneumococcal polysaccharides to induce significant immune response in a high proportion of HIV-infected patients.