Cytomegalovirus and other herpesviruses after hematopoietic cell and solid organ transplantation: From antiviral drugs to virus-specific T cells

被引:14
作者
Ivana, Tapuchova [1 ,2 ]
Robert, Pytlik [4 ]
Pavel, Simara [3 ,4 ]
Lenka, Tesarova [2 ,3 ]
Irena, Koutna [1 ,2 ,3 ]
机构
[1] Masaryk Univ, Fac Sci, Dept Expt Biol, Kamenice 5, Brno 62500, Czech Republic
[2] St Annes Univ Hosp Brno, Int Clin Res Ctr, Pekarska 53, Brno 65691, Czech Republic
[3] Masaryk Univ, Fac Med, Dept Histol & Embryol, Karnenice 3, Brno 62500, Czech Republic
[4] Inst Hematol & Blood Transfus, Cell Therapy Dept, U Nemocnice 2094-1, Prague 12800 2, Czech Republic
关键词
Virus-specific T cells; Herpesviruses; Adoptive transfer; Cytomegalovirus; Resistance; Interferon gamma; Immunotherapy; EPSTEIN-BARR-VIRUS; VARICELLA-ZOSTER-VIRUS; VERSUS-HOST-DISEASE; POSTTRANSPLANT LYMPHOPROLIFERATIVE DISORDER; SARCOMA-ASSOCIATED HERPESVIRUS; SEVERE VIRAL-INFECTIONS; RESISTANT CYTOMEGALOVIRUS; GANCICLOVIR-RESISTANT; RISK-FACTORS; IN-VITRO;
D O I
10.1016/j.trim.2022.101539
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Herpesviruses can either cause primary infection or may get reactivated after both hematopoietic cell and solid organ transplantations. In general, viral infections increase post-transplant morbidity and mortality. Prophylactic, preemptive, or therapeutically administered antiviral drugs may be associated with serious side effects and may induce viral resistance. Virus-specific T cells represent a valuable addition to antiviral treatment, with high rates of response and minimal side effects. Even low numbers of virus-specific T cells manufactured by direct selection methods can reconstitute virus-specific immunity after transplantation and control viral replication. Virus-specific T cells belong to the advanced therapy medicinal products, and their production is regulated by appropriate legislation; also, strict safety regulations are required to minimize their side effects.
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页数:13
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