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Comparison of Immune Response to Booster Vaccines in Blood Transplant Patients and Healthy Volunteers

Evaluation of Hepatitis B Surface Antigen-Specific and Tetanus Toxoid-Specific Lymphocytes

This study will compare the immune system response to booster vaccines for tetanus/diphtheria and hepatitis B in healthy volunteers with that of patients who have had a blood transplant. (A blood transplant is an infusion of donated stem cells-i.e., cells that mature into white blood cells, red blood cells and platelets). The study will also look at how age of the blood cell donor and recipient, the type of blood transplant, the amount of certain types of white cells in donor blood, and other variables may influence the vaccine response among the transplant patients.

This study includes normal volunteers and patients who have had a blood transplant. Healthy volunteers between the ages of 18 and 60 who have previously been vaccinated with the hepatitis B or tetanus/diphtheria vaccine and have not had hepatitis B may be eligible for this study. Patients enrolled in a blood cell transplant study at NIH who are between 5 and 60 years old, have been vaccinated against tetanus/diphtheria, and have not had hepatitis B may be eligible. Candidates will be screened with a medical history and blood tests.

Those enrolled in the study will have about 2 tablespoons of blood drawn before vaccination with a standard tetanus/diphtheria booster shot. Volunteers who have previously been vaccinated with the hepatitis B vaccine and all blood transplant patients will also receive a hepatitis B vaccination. Participants will have blood drawn (from 1 to 5 tablespoons) up to once a week after vaccination for no more than 8 weeks to evaluate the immune response to vaccination.

Studieoversikt

Status

Fullført

Detaljert beskrivelse

This study will compare booster vaccine responses in patients undergoing hematopoietic stem cell transplant (HSCT) to a group of healthy volunteers. Responses among different types of HSCT will be compared to each other as well. Serum antibody titers to vaccine antigens and quantification of antigen specific lymphocytes will be followed. Approximately 15 healthy subjects and 40 patients will be enrolled.

Studietype

Observasjonsmessig

Registrering

55

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Maryland
      • Bethesda, Maryland, Forente stater, 20892
        • National Institute of Allergy and Infectious Diseases (NIAID)

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

HEALTHY VOLUNTEERS:

Male or female subjects who are at least 18 years of age, but no older than 60 years of age.

Received complete hepatitis B and/or tetanus/diphtheria vaccination series.

If female, have a negative urine or serum pregnancy test within two weeks prior to entry into this study, and agree to avoid pregnancy during entire participation through the use of effective birth control or abstinence.

Volunteers reporting good general health and denying any illness that can adversely affect an immune response to a vaccine.

No history of a serious adverse event associated with any previous vaccination.

Not participating in another experimental vaccine study.

Serum hemoglobin greater than or equal to 11 g/dL.

No history of hepatitis B.

Must not have received a tetanus/diphtheria or hepatitis B booster in the last 6 months.

HSCT VOLUNTEERS:

Male or female subjects who are at least 5 years of age, but no older than 60 years of age.

Be enrolled in a HSCT protocol at NIH.

Be greater than or equal to 3 months post-HSCT.

Received tetanus/diphtheria vaccination series.

If female, have a negative urine or serum pregnancy test within two weeks prior to entry into this study, and agree to avoid pregnancy during entire participation through the use of effective birth control or abstinence.

No history of a serious adverse event associated with any previous vaccination.

Not participating in another experimental vaccine study.

Serum hemoglobin greater than or equal to 9 g/dL.

No history of hepatitis B.

Not receiving any more than replacement glucocorticoid therapy.

Not receiving any dose of cyclosporine.

No acute graft-versus-host disease grade II or higher, at time of consideration for study.

No chronic graft-versus-host disease more involved than localized skin lesions and/or liver dysfunction, at time of consideration for study.

Must not have received a tetanus/diphtheria or hepatitis B booster in the last 6 months.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. juni 2000

Studiet fullført

1. mai 2002

Datoer for studieregistrering

Først innsendt

9. juni 2000

Først innsendt som oppfylte QC-kriteriene

9. juni 2000

Først lagt ut (Anslag)

12. juni 2000

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

4. mars 2008

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. mars 2008

Sist bekreftet

1. mai 2002

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 000144
  • 00-I-0144

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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