Leen Ann M, Christin Anne, Myers Gary D, Liu Hao, Cruz Conrad R, Hanley Patrick J, Kennedy-Nasser Alana A, Leung Kathryn S, Gee Adrian P, Krance Robert A, Brenner Malcolm K, Heslop Helen E, Rooney Cliona M, Bollard Catherine M
Center for Cell and Gene Therapy and Departments of Pediatrics, Immunology, Medicine, and Virology, Baylor College of Medicine, Texas Children's Hospital and the Methodist Hospital, Houston, TX 77030, USA.
Blood. 2009 Nov 5;114(19):4283-92. doi: 10.1182/blood-2009-07-232454. Epub 2009 Aug 21.
Viral infection or reactivation remains a major cause of morbidity and mortality after allogeneic stem cell transplantation. We now show that infusions of single cytotoxic T lymphocyte (CTL) lines (5 x 10(6)-1.35 x 10(8) cells/m(2)) with specificity for 2 commonly detected viruses, Epstein-Barr virus (EBV) and adenovirus, can be safely administered to pediatric transplantation recipients receiving partially human leukocyte antigen-matched and haploidentical stem cell grafts (n = 13), without inducing graft-versus-host disease. The EBV-specific component of the CTLs expanded in vivo and persisted for more than 12 weeks, but the adenovirus-specific component only expanded in vivo in the presence of concomitant adenoviral infection. Nevertheless, adenovirus-specific T cells could be detected for at least 8 weeks in peripheral blood, even in CTL recipients without viral infection, provided the adenovirus-specific component of their circulating lymphocytes was first expanded by exposure to adenoviral antigens ex vivo. After infusion, none of these 13 high-risk recipients developed EBV-associated lymphoproliferative disease, while 2 of the subjects had resolution of their adenoviral disease. Hence, bispecific CTLs containing both EBV- and adenovirus-specific T cells can safely reconstitute an antigen responsive "memory" population of CTLs after human leukocyte antigen-mismatched stem cell transplantation and may provide antiviral activity. This trial was registered at www.clinicaltrials.gov as #NCT00590083.
病毒感染或再激活仍然是异基因干细胞移植后发病和死亡的主要原因。我们现在表明,向接受部分人类白细胞抗原匹配和单倍体相合干细胞移植的儿科移植受者(n = 13)安全输注对两种常见检测病毒——爱泼斯坦-巴尔病毒(EBV)和腺病毒具有特异性的单个细胞毒性T淋巴细胞(CTL)系(5×10⁶ - 1.35×10⁸ 个细胞/m²),不会诱发移植物抗宿主病。CTLs的EBV特异性成分在体内扩增并持续超过12周,但腺病毒特异性成分仅在伴有腺病毒感染时在体内扩增。然而,即使在没有病毒感染的CTL受者中,只要其循环淋巴细胞的腺病毒特异性成分首先通过体外暴露于腺病毒抗原而扩增,外周血中至少8周都能检测到腺病毒特异性T细胞。输注后,这13名高危受者均未发生EBV相关的淋巴增殖性疾病,而其中2名受试者的腺病毒疾病得到缓解。因此,含有EBV和腺病毒特异性T细胞的双特异性CTLs在人类白细胞抗原不相合的干细胞移植后可安全地重建抗原反应性“记忆”CTL群体,并可能提供抗病毒活性。该试验已在www.clinicaltrials.gov上注册,编号为#NCT00590083。