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Pertussis Immunity and Response to Tetanus-Reduced Diphtheria-Reduced Pertussis Vaccine (Tdap) after Autologous Peripheral Blood Stem Cell Transplantation
被引:31
|作者:
Small, Trudy N.
[1
]
Zelenetz, Andrew D.
[2
]
Noy, Ariela
[2
]
Rice, R. David
[3
]
Trippett, Tanya M.
Abrey, Lauren
[2
]
Portlock, Carol S.
[2
]
McCullagh, Emily J.
[3
]
Vanak, Jill M.
[3
]
Mulligan, Ann Marie
[3
]
Moskowitz, Craig H.
[2
]
机构:
[1] Mem Sloan Kettering Canc Ctr, Dept Pediat, Bone Marrow Transplant Serv, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Nursing, New York, NY 10021 USA
关键词:
Pertussis;
Transplantation;
Vaccination;
HIGH-DOSE THERAPY;
BONE-MARROW;
RECOMMENDATIONS;
IMMUNIZATION;
LYMPHOMA;
DISEASE;
D O I:
10.1016/j.bbmt.2009.07.018
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Pertussis is a highly contagious respiratory infection characterized by prolonged cough and inspiratory whoop. Despite widespread vaccination of children aged < 7 years, its incidence is steadily increasing in adolescents and adults, because of the known decrease in immunity following childhood immunization. In an effort to reduce pertussis in adolescents and adults, 2 vaccines containing tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) (BOOSTRIX and Adacel) were licensed in 2005 for use in adolescents, I of which (Adacel) contains less pertussis toxoid (PT) for use in adults. This study assessed pertussis titers in 57 adult survivors of an autologous peripheral blood stem cell transplantation (PBSCT; median age, 37.5 years), 28 of whom were subsequently vaccinated with Tdap containing 2.5 mu g of PT (Adacel). The median time to Tdap administration was 3 years posttransplantation. Before vaccination, 87% of the patients lacked pertussis immunity. Only 2 of the 28 patients developed a >2-fold response to PT following vaccination with Tdap. These data suggest that autologous transplantation recipients are highly susceptible to pertussis and that immunization with 2.5 mu g of PT induces an inadequate response. Prospective trials evaluating BOOSTRIX, containing 8 mu g/dose of PT (approved for adults in December 2008) are warranted in this vulnerable population undergoing transplantation. Biol Blood Marrow Transplant 15: 1538-1542 (2009) (C) 2009 American Society for Blood and Marrow Transplantation
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页码:1538 / 1542
页数:5
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