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Immunogenicity, safety, and predictors of response after a pneumococcal conjugate and pneumococcal polysaccharide vaccine series in human immunodeficiency virus-infected children receiving highly active antiretroviral therapy.
Pediatr Infect Dis J. 2006 Oct; 25(10):920-9.PI

Abstract

BACKGROUND

The immunogenicity and safety of 2 doses of pneumococcal conjugate vaccine (PCV) and 1 dose of pneumococcal polysaccharide vaccine (PPV) were evaluated in human immunodeficiency virus (HIV)-infected children receiving highly active antiretroviral therapy (HAART).

METHODS

Children 2 to <19 years, receiving stable HAART for > or =3-6 months, with HIV RNA PCR <30,000-60,000 copies/mL, received 2 doses of PCV and 1 dose of PPV at sequential 8-week intervals. Antibodies to pneumococcal serotypes (STs) 1 (PPV only) and 6B, 14, 19F, and 23F (PCV and PPV) were measured by ELISA.

RESULTS

Two hundred sixty-three subjects were enrolled, of whom 225 met criteria for inclusion in the primary dataset. Antibody concentrations were low at entry, despite previous PPV in 75%. After vaccination, 76%-96% had concentrations > or =0.5 microg/mL and 62-88% > or =1.0 microg/mL to the 5 STs (geometric mean concentrations [GMCs] = 1.44-4.25 microg/mL). Incremental gains in antibody concentration occurred with each vaccine dose. Predictors of response included higher antibody concentration at entry, higher immune stratum (based on nadir CD4% before HAART and CD4% at screening), lower entry viral RNA, longer duration of the entry HAART regimen, and age <7 years. Response was more consistently related to screening CD4% than nadir CD4%. Seven percent had vaccine-related grade 3 events, most of which were local reactions.

CONCLUSIONS

Two PCVs and 1 PPV were immunogenic and safe in HIV-infected children 2 to <19 years who were receiving HAART. Responses were suggestive of functional immune reconstitution. Immunologic status based on nadir and, especially, current CD4% and control of HIV viremia were independent determinants of response.

Authors+Show Affiliations

University of Colorado School of Medicine, Pediatric Infectious Disease, The Children's Hospital, Denver, CO 80218, USA. abzug.mark@tchden.orgNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

17006288

Citation

Abzug, Mark J., et al. "Immunogenicity, Safety, and Predictors of Response After a Pneumococcal Conjugate and Pneumococcal Polysaccharide Vaccine Series in Human Immunodeficiency Virus-infected Children Receiving Highly Active Antiretroviral Therapy." The Pediatric Infectious Disease Journal, vol. 25, no. 10, 2006, pp. 920-9.
Abzug MJ, Pelton SI, Song LY, et al. Immunogenicity, safety, and predictors of response after a pneumococcal conjugate and pneumococcal polysaccharide vaccine series in human immunodeficiency virus-infected children receiving highly active antiretroviral therapy. Pediatr Infect Dis J. 2006;25(10):920-9.
Abzug, M. J., Pelton, S. I., Song, L. Y., Fenton, T., Levin, M. J., Nachman, S. A., Borkowsky, W., Rosenblatt, H. M., Marcinak, J. F., Dieudonne, A., Abrams, E. J., & Pathak, I. (2006). Immunogenicity, safety, and predictors of response after a pneumococcal conjugate and pneumococcal polysaccharide vaccine series in human immunodeficiency virus-infected children receiving highly active antiretroviral therapy. The Pediatric Infectious Disease Journal, 25(10), 920-9.
Abzug MJ, et al. Immunogenicity, Safety, and Predictors of Response After a Pneumococcal Conjugate and Pneumococcal Polysaccharide Vaccine Series in Human Immunodeficiency Virus-infected Children Receiving Highly Active Antiretroviral Therapy. Pediatr Infect Dis J. 2006;25(10):920-9. PubMed PMID: 17006288.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Immunogenicity, safety, and predictors of response after a pneumococcal conjugate and pneumococcal polysaccharide vaccine series in human immunodeficiency virus-infected children receiving highly active antiretroviral therapy. AU - Abzug,Mark J, AU - Pelton,Stephen I, AU - Song,Lin-Ye, AU - Fenton,Terence, AU - Levin,Myron J, AU - Nachman,Sharon A, AU - Borkowsky,William, AU - Rosenblatt,Howard M, AU - Marcinak,John F, AU - Dieudonne,Arry, AU - Abrams,Elaine J, AU - Pathak,Indu, AU - ,, PY - 2006/9/29/pubmed PY - 2006/12/21/medline PY - 2006/9/29/entrez SP - 920 EP - 9 JF - The Pediatric infectious disease journal JO - Pediatr Infect Dis J VL - 25 IS - 10 N2 - BACKGROUND: The immunogenicity and safety of 2 doses of pneumococcal conjugate vaccine (PCV) and 1 dose of pneumococcal polysaccharide vaccine (PPV) were evaluated in human immunodeficiency virus (HIV)-infected children receiving highly active antiretroviral therapy (HAART). METHODS: Children 2 to <19 years, receiving stable HAART for > or =3-6 months, with HIV RNA PCR <30,000-60,000 copies/mL, received 2 doses of PCV and 1 dose of PPV at sequential 8-week intervals. Antibodies to pneumococcal serotypes (STs) 1 (PPV only) and 6B, 14, 19F, and 23F (PCV and PPV) were measured by ELISA. RESULTS: Two hundred sixty-three subjects were enrolled, of whom 225 met criteria for inclusion in the primary dataset. Antibody concentrations were low at entry, despite previous PPV in 75%. After vaccination, 76%-96% had concentrations > or =0.5 microg/mL and 62-88% > or =1.0 microg/mL to the 5 STs (geometric mean concentrations [GMCs] = 1.44-4.25 microg/mL). Incremental gains in antibody concentration occurred with each vaccine dose. Predictors of response included higher antibody concentration at entry, higher immune stratum (based on nadir CD4% before HAART and CD4% at screening), lower entry viral RNA, longer duration of the entry HAART regimen, and age <7 years. Response was more consistently related to screening CD4% than nadir CD4%. Seven percent had vaccine-related grade 3 events, most of which were local reactions. CONCLUSIONS: Two PCVs and 1 PPV were immunogenic and safe in HIV-infected children 2 to <19 years who were receiving HAART. Responses were suggestive of functional immune reconstitution. Immunologic status based on nadir and, especially, current CD4% and control of HIV viremia were independent determinants of response. SN - 0891-3668 UR - https://www.unboundmedicine.com/medline/citation/17006288/Immunogenicity_safety_and_predictors_of_response_after_a_pneumococcal_conjugate_and_pneumococcal_polysaccharide_vaccine_series_in_human_immunodeficiency_virus_infected_children_receiving_highly_active_antiretroviral_therapy_ DB - PRIME DP - Unbound Medicine ER -