Immunogenicity of a prophylactic quadrivalent human papillomavirus L1 virus-like particle vaccine in male and female adolescent transplant recipients.

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Citation: Pediatric Transplantation. 18(3):310-5, 2014 May.PMID: 24484551Institution: MedStar Washington Hospital CenterDepartment: Obstetrics and Gynecology/Pediatric and AdolescentForm of publication: Journal ArticleMedline article type(s): Clinical Trial | Journal Article | Research Support, Non-U.S. Gov'tSubject headings: *Kidney/vi [Virology] | *Liver/vi [Virology] | *Papillomavirus Infections/pc [Prevention & Control] | *Papillomavirus Vaccines/tu [Therapeutic Use] | *Vaccines, Virus-Like Particle/tu [Therapeutic Use] | Adolescent | Antibodies, Viral/bl [Blood] | Antibody Formation | Child | Female | Human papillomavirus 11/im [Immunology] | Humans | Immunoassay | Immunosuppressive Agents/tu [Therapeutic Use] | Kidney Transplantation | Liver Failure/co [Complications] | Liver Failure/su [Surgery] | Liver Failure/vi [Virology] | Liver Transplantation | Male | Renal Insufficiency/co [Complications] | Renal Insufficiency/su [Surgery] | Renal Insufficiency/vi [Virology] | Transplant Recipients | VaccinationISSN:
  • 1397-3142
Name of journal: Pediatric transplantationAbstract: Organ TX recipients are at an increased risk of developing cancers of the lower genital tract related to HPV. The quadrivalent HPV vaccine has high efficacy in preventing these diseases, but response to many vaccines is suboptimal after organ transplantation. Liver and kidney TX recipients received quadrivalent HPV vaccine. Serum samples were tested for anti-HPV levels. Of 20 renal transplant recipients screened, 14 received vaccine. Of these, seven completed the vaccine series and seven had incomplete vaccination. Of five liver TX children, three received vaccines (two complete and one incomplete). All eight kidney and liver TX children with complete vaccination and available results were seronegative at baseline and had seroconversion at month 7 for all four HPV types. Six of 14 (42.8%) kidney TX recipients developed AR. During the same time period, eight of 28 (28.5%) non-vaccine renal transplant recipients developed AR (p = ns). Transplant adolescents developed 100% seroconversion to all four HPV serotypes with HPV vaccine with serologic titers similar to historic controls. A non-significant increased incidence of AR was noted among kidney transplant vaccine recipients. A much larger study would be needed to evaluate whether HPV vaccination increases AR in transplant adolescents.Copyright � 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.All authors: Gomez-Lobo V, Kaufman S, Moudgil A, Torres C, Whyte TDigital Object Identifier: Date added to catalog: 2015-03-17
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Journal Article MedStar Authors Catalog Article Available 24484551

Organ TX recipients are at an increased risk of developing cancers of the lower genital tract related to HPV. The quadrivalent HPV vaccine has high efficacy in preventing these diseases, but response to many vaccines is suboptimal after organ transplantation. Liver and kidney TX recipients received quadrivalent HPV vaccine. Serum samples were tested for anti-HPV levels. Of 20 renal transplant recipients screened, 14 received vaccine. Of these, seven completed the vaccine series and seven had incomplete vaccination. Of five liver TX children, three received vaccines (two complete and one incomplete). All eight kidney and liver TX children with complete vaccination and available results were seronegative at baseline and had seroconversion at month 7 for all four HPV types. Six of 14 (42.8%) kidney TX recipients developed AR. During the same time period, eight of 28 (28.5%) non-vaccine renal transplant recipients developed AR (p = ns). Transplant adolescents developed 100% seroconversion to all four HPV serotypes with HPV vaccine with serologic titers similar to historic controls. A non-significant increased incidence of AR was noted among kidney transplant vaccine recipients. A much larger study would be needed to evaluate whether HPV vaccination increases AR in transplant adolescents.Copyright � 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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