Restoration of immunity in lymphopenic individuals with cancer by vaccination and adoptive T-cell transfer

被引:235
作者
Rapoport, AP
Stadtmauer, EA
Aqui, N
Badros, A
Cotte, J
Chrisley, L
Veloso, E
Zheng, ZH
Westphal, S
Mair, R
Chi, N
Ratterree, B
Pochran, MF
Natt, S
Hinkle, J
Sickles, C
Sohal, A
Ruehle, K
Lynch, C
Zhang, L
Porter, DL
Luger, S
Guo, CF
Fang, HB
Blackwelder, W
Hankey, K
Mann, D
Edelman, R
Frasch, C
Levine, BL
Cross, A
June, CH
机构
[1] Univ Maryland, Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[2] Univ Maryland, Ctr Vaccine Dev, Baltimore, MD 21201 USA
[3] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[4] US FDA, Ctr Biol Evolut & Res, Rockville, MD 20852 USA
关键词
D O I
10.1038/nm1310
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Immunodeficiency is a barrier to successful vaccination in individuals with cancer and chronic infection. We performed a randomized phase 1/2 study in lymphopenic individuals after high-dose chemotherapy and autologous hematopoietic stem cell transplantation for myeloma. Combination immunotherapy consisting of a single early post-transplant infusion of in vivo vaccine-primed and ex vivo costimulated autologous T cells followed by post-transplant booster immunizations improved the severe immunodeficiency associated with high-dose chemotherapy and led to the induction of clinically relevant immunity in adults within a month after transplantation. Immune assays showed accelerated restoration of CD4 T-cell numbers and function. Early T-cell infusions also resulted in significantly improved T-cell proliferation in response to antigens that were not contained in the vaccine, as assessed by responses to staphylococcal enterotoxin B and cytomegalovirus antigens ( P < 0.05). In the setting of lymphopenia, combined vaccine therapy and adoptive T-cell transfer fosters the development of enhanced memory T-cell responses.
引用
收藏
页码:1230 / 1237
页数:8
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