Abstract
These studies were performed to assess the utility of the baboon as a nonhuman primate model to evaluate vaccines for use in humans. Specifically, we examined the antibody response of baboons immunized during the third trimester of pregnancy with Haemophilus influenzae type b (Hib) polyribosylribitol phosphate (PRP) conjugate and unconjugated polysaccharide vaccines. Some of the vaccinated mothers failed to respond to a single immunization with unconjugated Hib PRP. Specific Hib PRP immunoglobulin G (IgG) but not IgM antibodies cross the baboon placenta and are detected in the offspring. Higher-titer baboon anti-Hib PRP did not express two previously defined cross-reactive human anti-Hib PRP idiotypes and was biased towards lambda light-chain expression. Spectrotype analysis indicated that baboon anti-Hib PRP was restricted in heterogeneity and oligoclonal.
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- Attanasio R., Allan J. S., Anderson S. A., Chanh T. C., Kennedy R. C. Anti-idiotypic antibody response to monoclonal anti-CD4 preparations in nonhuman primate species. J Immunol. 1991 Jan 15;146(2):507–514. [PubMed] [Google Scholar]
- Baker C. J. Immunization to prevent group B streptococcal disease: victories and vexations. J Infect Dis. 1990 May;161(5):917–921. doi: 10.1093/infdis/161.5.917. [DOI] [PubMed] [Google Scholar]
- Chen S. T., Edsall G., Peel M. M., Sinnathuray T. A. Timing of antenatal tetanus immunization for effective protection of the neonate. Bull World Health Organ. 1983;61(1):159–165. [PMC free article] [PubMed] [Google Scholar]
- Damian R. T., Greene N. D., Kalter S. S. IgG subclasses in the baboon (Papio cynocephalus). J Immunol. 1971 Jan;106(1):246–257. [PubMed] [Google Scholar]
- Del Portillo H. A., Schmidt G. W., Damian R. T. Immunochemical analysis of baboon (Papio cynocephalus) IgG subclasses. Vet Immunol Immunopathol. 1987 Nov;16(3-4):201–214. doi: 10.1016/0165-2427(87)90018-3. [DOI] [PubMed] [Google Scholar]
- Englund J. A., Glezen W. P., Turner C., Harvey J., Thompson C., Siber G. R. Transplacental antibody transfer following maternal immunization with polysaccharide and conjugate Haemophilus influenzae type b vaccines. J Infect Dis. 1995 Jan;171(1):99–105. doi: 10.1093/infdis/171.1.99. [DOI] [PubMed] [Google Scholar]
- Granoff D. M., Shackelford P. G., Pandey J. P., Boies E. G. Antibody responses to Haemophilus influenzae type b polysaccharide vaccine in relation to Km(1) and G2m(23) immunoglobulin allotypes. J Infect Dis. 1986 Aug;154(2):257–264. doi: 10.1093/infdis/154.2.257. [DOI] [PubMed] [Google Scholar]
- Hankins G. D., Lowery C. L., Jr, Scott R. T., Morrow W. R., Carey K. D., Leland M. M., Colvin E. V. Transplacental transfer of zidovudine in the near-term pregnant baboon. Am J Obstet Gynecol. 1990 Sep;163(3):728–732. doi: 10.1016/0002-9378(90)91057-j. [DOI] [PubMed] [Google Scholar]
- Kim K. H., Park M. K., Peeters C. C., Poolman J. T., Shearer M. H., Kennedy R. C., Nahm M. H. Comparison of nonhuman primate antibodies against Haemophilus influenzae type b polysaccharide with human antibodies in oligoclonality and in vivo protective potency. Infect Immun. 1994 Jun;62(6):2426–2431. doi: 10.1128/iai.62.6.2426-2431.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lucas A. H., Azmi F. H., Mink C. M., Granoff D. M. Age-dependent V region expression in the human antibody response to the Haemophilus influenzae type b polysaccharide. J Immunol. 1993 Mar 1;150(5):2056–2061. [PubMed] [Google Scholar]
- Lucas A. H. Expression of crossreactive idiotypes by human antibodies specific for the capsular polysaccharide of Hemophilus influenzae B. J Clin Invest. 1988 Feb;81(2):480–486. doi: 10.1172/JCI113345. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lucas A. H., Granoff D. M. A major crossreactive idiotype associated with human antibodies to the Haemophilus influenzae b polysaccharide. Expression in relation to age and immunoglobulin G subclass. J Clin Invest. 1990 Apr;85(4):1158–1166. doi: 10.1172/JCI114548. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Martin L. N. Chromatographic fractionation of rhesus monkey (Macaca mulatta) IgG subclasses using deae cellulose and protein A-sepharose. J Immunol Methods. 1982;50(3):319–329. doi: 10.1016/0022-1759(82)90170-3. [DOI] [PubMed] [Google Scholar]
- Pauerstein C. J., Eddy C. A., Croxatto H. D., Hess R., Siler-Khodr T. M., Croxatto H. B. Temporal relationships of estrogen, progesterone, and luteinizing hormone levels to ovulation in women and infrahuman primates. Am J Obstet Gynecol. 1978 Apr 15;130(8):876–886. doi: 10.1016/0002-9378(78)90264-8. [DOI] [PubMed] [Google Scholar]
- Rahman M., Chen L. C., Chakraborty J., Yunus M., Chowdhury A. I., Sarder A. M., Bhatia S., Curlin G. T. Use of tetanus toxoid for the prevention of neonatal tetanus. 1. Reduction of neonatal mortality by immunization of non-pregnant and pregnant women in rural Bangladesh. Bull World Health Organ. 1982;60(2):261–267. [PMC free article] [PubMed] [Google Scholar]
- Robbins J. B., Parke J. C., Jr, Schneerson R., Whisnant J. K. Quantitative measurement of "natural" and immunization-induced Haemophilus influenzae type b capsular polysaccharide antibodies. Pediatr Res. 1973 Mar;7(3):103–110. doi: 10.1203/00006450-197303000-00001. [DOI] [PubMed] [Google Scholar]
- SCHOFIELD F. D., TUCKER V. M., WESTBROOK G. R. Neonatal tetanus in New Guinea. Effect of active immunization in pregnancy. Br Med J. 1961 Sep 23;2(5255):785–789. doi: 10.1136/bmj.2.5255.785. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shearer M. H., Jenson H. B., Carey K. D., Chanh T. C., Kennedy R. C. Production and characterization of murine monoclonal antibodies specific for baboon IgG heavy and light chain epitopes. J Med Primatol. 1994 Sep;23(7):382–387. doi: 10.1111/j.1600-0684.1994.tb00124.x. [DOI] [PubMed] [Google Scholar]
- Shearer M. H., Stevens F. J., Westholm F. A., Jenson H. B., Chanh T. C., Carey K. D., White G. L., 2nd, Solomon A., Kennedy R. C., 2nd Serologic crossreactions among primate immunoglobulins. Dev Comp Immunol. 1995 Nov-Dec;19(6):547–557. doi: 10.1016/0145-305x(95)00026-p. [DOI] [PubMed] [Google Scholar]
- Stevens V. C., Sparks S. J., Powell J. E. Levels of estrogens, progestogens and luteinizing hormone during the menstrual cycle of the baboon. Endocrinology. 1970 Oct;87(4):658–666. doi: 10.1210/endo-87-4-658. [DOI] [PubMed] [Google Scholar]
- Wolf H., Warren R. Q., Stunz G. W., Shuler K. R., Kanda P., Kennedy R. C. Fine specificity of the murine antibody response to HIV-1 gp160 determined by synthetic peptides which define selected epitopes. Mol Immunol. 1992 Jul-Aug;29(7-8):989–998. doi: 10.1016/0161-5890(92)90138-n. [DOI] [PubMed] [Google Scholar]
- Yamamoto Y., Manyon A. T., Osawa Y., Kirdani R. Y., Sandberg A. A. Androgen metabolism in the baboon: a comparison with the human. J Steroid Biochem. 1978 Aug;9(8):751–759. doi: 10.1016/0022-4731(78)90195-4. [DOI] [PubMed] [Google Scholar]