Advances in HIV-1-specific chimeric antigen receptor cells to target the HIV-1 reservoir

被引:3
作者
Choudhary, Madhu C. [1 ]
Cyktor, Joshua C. [1 ]
Riddler, Sharon A. [1 ]
机构
[1] Univ Pittsburgh, Div Infect Dis, Sch Med, Pittsburgh, PA 15213 USA
关键词
HIV-1; CAR T; CAR NK; ART-free remission; NATURAL-KILLER-CELLS; CD4; BINDING-SITE; CD8(+) T-CELLS; IN-VIVO; CAR; INFECTION; SURVIVAL; EXPRESSION; CD4-ZETA; PROLIFERATION;
D O I
10.1016/j.jve.2022.100073
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antiretroviral therapy (ART) for HIV-1 has dramatically improved outcomes for people living with HIV-1 but requires life-long adherence and can be associated with short and long-term toxicity. Numerous pre-clinical and clinical investigations are underway to develop therapies for immune control of HIV-1 in the absence of ART. The success of chimeric antigen receptor (CAR) cell therapy for hematological malignancy has renewed efforts to develop and investigate CAR cells as strategies to enhance HIV-1 immunity, enable virus control or elimination, and allow ART-free HIV-1 remission. Here, we review the improvements in anti-HIV-1 CAR cell therapy in the two decades since their initial clinical trials were conducted, describe the additional engineering required to protect CAR cells from HIV-1 infection, and preview the current landscape of CAR cell therapies advancing to HIV-1 clinical trials.
引用
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页数:8
相关论文
共 82 条
[1]   Defective killing activity against gp120/41-expressing human erythroleukaemic K562 cell line by monocytes and natural killer cells from HIV-infected individuals [J].
Ahmad, A ;
Menezes, J .
AIDS, 1996, 10 (02) :143-149
[2]   HIV-1-Specific Chimeric Antigen Receptors Based on Broadly Neutralizing Antibodies [J].
Ali, Ayub ;
Kitchen, Scott G. ;
Chen, Irvin S. Y. ;
Ng, Hwee L. ;
Zack, Jerome A. ;
Yang, Otto O. .
JOURNAL OF VIROLOGY, 2016, 90 (15) :6999-7006
[3]   Sequential deregulation of NK cell subset distribution and function starting in acute HIV-1 infection [J].
Alter, G ;
Teigen, N ;
T Davis, B ;
Addo, MM ;
Suscovich, TJ ;
Waring, MT ;
Streeck, H ;
Johnston, MN ;
Staller, KD ;
Zaman, MT ;
Yu, XG ;
Lichterfeld, M ;
Basgoz, N ;
Rosenberg, ES ;
Altfeld, M .
BLOOD, 2005, 106 (10) :3366-3369
[4]   Multispecific anti-HIV duoCAR-T cells display broad in vitro antiviral activity and potent in vivo elimination of HIV-infected cells in a humanized mouse model [J].
Anthony-Gonda, Kim ;
Bardhi, Ariola ;
Ray, Alex ;
Flerin, Nina ;
Li, Mengyan ;
Chen, Weizao ;
Ochsenbauer, Christina ;
Kappes, John C. ;
Krueger, Winfried ;
Worden, Andrew ;
Schneider, Dina ;
Zhu, Zhongyu ;
Orentas, Rimas ;
Dimitrov, Dimiter S. ;
Goldstein, Harris ;
Dropulic, Boro .
SCIENCE TRANSLATIONAL MEDICINE, 2019, 11 (504)
[5]   Stem cell-derived CAR T cells traffic to HIV reservoirs in macaques [J].
Barber-Axthelm, Isaac M. ;
Barber-Axthelm, Valerie ;
Sze, Kai Yin ;
Zhen, Anjie ;
Suryawanshi, Gajendra W. ;
Chen, Irvin S. Y. ;
Zack, Jerome A. ;
Kitchen, Scott G. ;
Kiem, Hans-Peter ;
Peterson, Christopher W. .
JCI INSIGHT, 2021, 6 (01)
[6]   Trivalent CAR T cells overcome interpatient antigenic variability in glioblastoma [J].
Bielamowicz, Kevin ;
Fousek, Kristen ;
Byrd, Tiara T. ;
Samaha, Hebatalla ;
Mukherjee, Malini ;
Aware, Nikita ;
Wu, Meng-Fen ;
Orange, Jordan S. ;
Sumazin, Pavel ;
Man, Tsz-Kwong ;
Joseph, Sujith K. ;
Hegde, Meenakshi ;
Ahmed, Nabil .
NEURO-ONCOLOGY, 2018, 20 (04) :506-518
[7]  
Bitton N, 1998, EUR J IMMUNOL, V28, P4177, DOI 10.1002/(SICI)1521-4141(199812)28:12<4177::AID-IMMU4177>3.0.CO
[8]  
2-J
[9]   Novel cellular therapies for leukemia: CAR-modified T cells targeted to the CD19 antigen [J].
Brentjens, Renier J. ;
Curran, Kevin J. .
HEMATOLOGY-AMERICAN SOCIETY OF HEMATOLOGY EDUCATION PROGRAM, 2012, :143-151
[10]   SIGNALS THROUGH T-CELL RECEPTOR-ZETA CHAIN ALONE ARE INSUFFICIENT TO PRIME RESTING T-LYMPHOCYTES [J].
BROCKER, T ;
KARJALAINEN, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1653-1659