中国全科医学 ›› 2022, Vol. 25 ›› Issue (11): 1393-1398.DOI: 10.12114/j.issn.1007-9572.2021.01.312
所属专题: 肿瘤最新文章合辑
杨蕾伊, 林桑, 谢其冰, 尹耕*
收稿日期:
2021-04-13
修回日期:
2021-10-27
出版日期:
2022-04-15
发布日期:
2022-03-28
通讯作者:
尹耕
基金资助:
Current Status of PD-1/PD-L1 Anti-tumor Therapy and Exploration of the Mechanism of Immune-related Adverse Events
YANG Leiyi,LIN Sang,XIE Qibing,YIN Geng*
Department of Rheumatology and Immunology,West China Hospital,Sichuan University,Chengdu 610041,China
* Corresponding author:YIN Geng,Chief physician;E-mail:yingeng1975@163.com
Received:
2021-04-13
Revised:
2021-10-27
Published:
2022-04-15
Online:
2022-03-28
摘要: 程序性细胞死亡蛋白-1(PD-1)和程序性细胞死亡配体1(PD-L1)抑制剂是一组免疫检查点抑制剂,自2006年5月起,已经有10种靶向PD-1和PD-L1的免疫检查点抑制剂用于肿瘤治疗。尽管PD-1和PD-L1抑制剂对某些肿瘤显示出良好的治疗效果,但是严重的免疫相关不良反应限制了其临床应用。因此,研发同等疗效但不良反应较PD-1/PD-L1抑制剂少的新型药物迫在眉睫。此外,探索免疫相关不良反应的发生机制可以为制定个性化的干预策略提供依据,在PD-1和PD-L1抑制剂研究中的地位同样重要。本综述讨论了几种抗PD-1/PD-L1单克隆抗体的作用机制及免疫相关不良反应,旨在提醒临床医生在进行抗肿瘤治疗的同时需要监控相关不良反应的发生。此外,本综述还指出了未来PD-1/PD-L1抑制剂可能的研究方向。
中图分类号:
YANG Leiyi, LIN Sang, XIE Qibing, YIN Geng.
Current Status of PD-1/PD-L1 Anti-tumor Therapy and Exploration of the Mechanism of Immune-related Adverse Events [J]. Chinese General Practice, 2022, 25(11): 1393-1398.
不良反应 | Pembrolizumab[ | Nivolumab[ | Cemiplimab[ | Toripalimab[ | Sintilimab[ | Camrelizumab[ | Atezolizumab[ | Durvalumab[ |
---|---|---|---|---|---|---|---|---|
甲状腺功能减退 | 14.3% | 0.3% | 10.2% | 12.1% | 20% | 22.2% | 0.32% | - |
甲状腺功能亢进 | 10.2% | 0.1% | - | - | - | - | - | - |
垂体炎 | 2.2% | 0.4% | - | - | - | - | - | - |
1型糖尿病 | 1.0% | 0.1% | - | - | 0 | - | - | 0.21% |
肾上腺功能不全 | 1.0% | - | - | - | - | - | - | - |
肺炎或间质性肺疾病 | 3.3% | 1.0% | 7.7% | 8.6% | 11% | 2.2% | - | 3.58% |
严重皮肤反应 | 0.6% | 0.3% | 1.3% | 0 | 0 | 0 | 0.32% | - |
自身免疫性肝炎 | 1.8% | 0.8% | 1.3% | - | - | - | 0.32% | - |
结肠炎 | 3.7% | 0.7% | 1.3% | - | - | - | 0.32% | - |
胰腺炎 | 0.4% | - | - | - | - | - | - | - |
肾炎 | 0.4% | 0.9% | - | - | - | - | 1.61% | 0.42% |
葡萄膜炎 | 0.4% | - | - | - | - | - | - | - |
心肌炎 | 0.2% | 0.1% | 1.3% | - | 1% | - | - | 0.42% |
血小板减少 | - | - | - | 8.6% | 10% | 17.7% | - | - |
表1 抗PD-1/PD-L1单克隆抗体治疗后诱发的部分免疫相关不良反应
Table 1 Some immune-related adverse events induced by PD-1/PD-L1 monoclonal antibody therapy
不良反应 | Pembrolizumab[ | Nivolumab[ | Cemiplimab[ | Toripalimab[ | Sintilimab[ | Camrelizumab[ | Atezolizumab[ | Durvalumab[ |
---|---|---|---|---|---|---|---|---|
甲状腺功能减退 | 14.3% | 0.3% | 10.2% | 12.1% | 20% | 22.2% | 0.32% | - |
甲状腺功能亢进 | 10.2% | 0.1% | - | - | - | - | - | - |
垂体炎 | 2.2% | 0.4% | - | - | - | - | - | - |
1型糖尿病 | 1.0% | 0.1% | - | - | 0 | - | - | 0.21% |
肾上腺功能不全 | 1.0% | - | - | - | - | - | - | - |
肺炎或间质性肺疾病 | 3.3% | 1.0% | 7.7% | 8.6% | 11% | 2.2% | - | 3.58% |
严重皮肤反应 | 0.6% | 0.3% | 1.3% | 0 | 0 | 0 | 0.32% | - |
自身免疫性肝炎 | 1.8% | 0.8% | 1.3% | - | - | - | 0.32% | - |
结肠炎 | 3.7% | 0.7% | 1.3% | - | - | - | 0.32% | - |
胰腺炎 | 0.4% | - | - | - | - | - | - | - |
肾炎 | 0.4% | 0.9% | - | - | - | - | 1.61% | 0.42% |
葡萄膜炎 | 0.4% | - | - | - | - | - | - | - |
心肌炎 | 0.2% | 0.1% | 1.3% | - | 1% | - | - | 0.42% |
血小板减少 | - | - | - | 8.6% | 10% | 17.7% | - | - |
[1] | FRANCISCO L M,SAGE P T,SHARPE A H. The PD-1 pathway in tolerance and autoimmunity[J]. Immunol Rev,2010,236:219-242. DOI:10.1111/j.1600-065X.2010.00923.x. |
[2] | OKAZAKI T,IWAI Y,HONJO T. New regulatory co-receptors:inducible co-Stimulator and PD-1[J]. Curr Opin Immunol,2002,14(6):779-782. DOI:10.1016/s0952-7915(02)00398-9. |
[3] | GIANCHECCHI E,DELFINO D V,FIERABRACCI A. Recent insights into the role of the PD-1/PD-L1 pathway in immunological tolerance and autoimmunity[J]. Autoimmun Rev,2013,12(11):1091-1100. DOI:10.1016/j.autrev.2013.05.003. |
[4] | LI Y Y,LIANG Z D,TIAN Y,et al. High-affinity PD-1 molecules deliver improved interaction with PD-L1 and PD-L2[J].Cancer Sci,2018,109(8):2435-2445. DOI:10.1111/cas.13666. |
[5] | NAKAMURA Y. Biomarkers for immune checkpoint inhibitor-mediated tumor response and adverse events[J]. Front Med (Lausanne),2019,6:119. DOI:10.3389/fmed.2019.00119. |
[6] | KWOK G,YAU T C,CHIU J W,et al. Pembrolizumab (keytruda)[J]. Hum Vaccin Immunother,2016,12(11):2777-2789. DOI:10.1080/21645515.2016.1199310. |
[7] | YAO S,CHEN L. PD-1 as an immune modulatory receptor[J].Cancer J,2014,20(4):262-264. DOI:10.1097/ppo.0000000000000060. |
[8] | LATCHMAN Y,WOOD C R,CHERNOVA T,et al. PD-L2 is a second ligand for PD-1 and inhibits T cell activation[J]. Nat Immunol,2001,2(3):261-268. DOI:10.1038/85330. |
[9] | MARASCO M,BERTEOTTI A,WEYERSHAEUSER J,et al. Molecular mechanism of SHP2 activation by PD-1 stimulation[J]. Sci Adv,2020,6(5):eaay4458. DOI:10.1126/sciadv.aay4458. |
[10] | CHAMOTO K,AL-HABSI M,HONJO T. Role of PD-1 in immunity and diseases[J]. Curr Top Microbiol Immunol,2017,410:75-97. DOI:10.1007/82_2017_67. |
[11] | DAI S,JIA R,ZHANG X,et al. The PD-1/PD-Ls pathway and autoimmune diseases[J]. Cell Immunol,2014,290(1):72-79. DOI:10.1016/j.cellimm.2014.05.006. |
[12] | ZOU W P,CHEN L P. Inhibitory B7-family molecules in the tumour microenvironment[J]. Nat Rev Immunol,2008,8(6):467-477. DOI:10.1038/nri2326. |
[13] | BUTTE M J,KEIR M E,PHAMDUY T B,et al. Programmed death-1 ligand 1 interacts specifically with the B7-1 costimulatory molecule to inhibit T cell responses[J]. Immunity,2007,27(1):111-122. DOI:10.1016/j.immuni.2007.05.016. |
[14] | OHAEGBULAM K C,ASSAL A,LAZAR-MOLNAR E,et al. Human cancer immunotherapy with antibodies to the PD-1 and PD-L1 pathway[J]. Trends Mol Med,2015,21(1):24-33. DOI:10.1016/j.molmed.2014.10.009. |
[15] | SCAPIN G,YANG X Y,PROSISE W W,et al. Structure of full-length human anti-PD1 therapeutic IgG4 antibody pembrolizumab[J]. Nat Struct Mol Biol,2015,22(12):953-958. DOI:10.1038/nsmb.3129. |
[16] | AHAMADI M,FRESHWATER T,PROHN M,et al. Model-based characterization of the pharmacokinetics of pembrolizumab:a humanized anti-PD-1 monoclonal antibody in advanced solid tumors[J]. CPT Pharmacometrics Syst Pharmacol,2017,6(1):49-57. DOI:10.1002/psp4.12139. |
[17] | PAZ-ARES L,LUFT A,VICENTE D,et al. Pembrolizumab plus chemotherapy for squamous non-small-cell lung cancer[J]. N Engl J Med,2018,379(21):2040-2051. DOI:10.1056/NEJMoa1810865. |
[18] | GANDHI L,RODRÍGUEZ-ABREU D,GADGEEL S,et al. Pembrolizumab plus chemotherapy in metastatic non-small-cell lung cancer[J]. N Engl J Med,2018,378(22):2078-2092. DOI:10.1056/NEJMoa1801005. |
[19] | MOK T S K,WU Y L,KUDABA I,et al. Pembrolizumab versus chemotherapy for previously untreated,PD-L1-expressing,locally advanced or metastatic non-small-cell lung cancer (KEYNOTE-042):a randomised,open-label,controlled,phase 3 trial[J]. Lancet,2019,393(10183):1819-1830. DOI:10.1016/S0140-6736(18)32409-7. |
[20] | BURTNESS B,HARRINGTON K J,GREIL R,et al. Pembrolizumab alone or with chemotherapy versus cetuximab with chemotherapy for recurrent or metastatic squamous cell carcinoma of the head and neck (KEYNOTE-048):a randomised,open-label,phase 3 study[J]. Lancet,2019,394(10212):1915-1928. DOI:10.1016/S0140-6736(19)32591-7. |
[21] | IWAI Y,HAMANISHI J,CHAMOTO K,et al. Cancer immunotherapies targeting the PD-1 signaling pathway[J]. J Biomed Sci,2017,24(1):26. DOI:10.1186/s12929-017-0329-9. |
[22] | BRAHMER J R,DRAKE C G,WOLLNER I,et al. Phase I study of single-agent anti-programmed death-1 (MDX-1106) in refractory solid tumors:safety,clinical activity,pharmacodynamics,and immunologic correlates[J]. J Clin Oncol,2010,28(19):3167-3175. DOI:10.1200/jco.2009.26.7609. |
[23] | HODI F S,O'DAY S J,MCDERMOTT D F,et al. Improved survival with ipilimumab in patients with metastatic melanoma[J]. N Engl J Med,2010,363(8):711-723. DOI:10.1056/nejmoa1003466. |
[24] | TOPALIAN S L,HODI F S,BRAHMER J R,et al. Safety,activity,and immune correlates of anti-PD-1 antibody in cancer[J]. N Engl J Med,2012,366(26):2443-2454. DOI:10.1056/NEJMoa1200690. |
[25] | ROBERT C,SCHACHTER J,LONG G V,et al. Pembrolizumab versus ipilimumab in advanced melanoma[J]. N Engl J Med,2015,372(26):2521-2532. DOI:10.1056/NEJMoa1503093. |
[26] | OVERMAN M J,LONARDI S,WONG K Y M,et al. Durable clinical benefit with nivolumab plus ipilimumab in DNA mismatch repair-deficient/microsatellite instability-high metastatic colorectal cancer[J]. J Clin Oncol,2018,36(8):773-779. DOI:10.1200/JCO.2017.76.9901. |
[27] | MOTZER R J,RINI B I,MCDERMOTT D F,et al. Nivolumab plus ipilimumab versus sunitinib in first-line treatment for advanced renal cell carcinoma:extended follow-up of efficacy and safety results from a randomised,controlled,phase 3 trial[J]. Lancet Oncol,2019,20(10):1370-1385. DOI:10.1016/S1470-2045(19)30413-9. |
[28] | HELLMANN M D,PAZ-ARES L,BERNABE CARO R,et al. Nivolumab plus ipilimumab in advanced non-small-cell lung cancer[J]. N Engl J Med,2019,381(21):2020-2031. DOI:10.1056/nejmoa1910231. |
[29] | HELLMANN M D,CIULEANU T E,PLUZANSKI A,et al. Nivolumab plus ipilimumab in lung cancer with a high tumor mutational burden[J]. N Engl J Med,2018,378(22):2093-2104. DOI:10.1056/NEJMoa1801946. |
[30] | AHMED S R,PETERSEN E,PATEL R,et al. Cemiplimab-rwlc as first and only treatment for advanced cutaneous squamous cell carcinoma[J]. Expert Rev Clin Pharmacol,2019,12(10):947-951. DOI:10.1080/17512433.2019.1665026. |
[31] | KAPLON H,REICHERT J M. Antibodies to watch in 2018[J]. MAbs,2018,10(2):183-203. DOI:10.1080/19420862.2018.1415671. |
[32] | AI L L,CHEN J,YAN H,et al. Research status and outlook of PD-1/PD-L1 inhibitors for cancer therapy[J]. Drug Des Devel Ther,2020,14:3625-3649. DOI:10.2147/DDDT.S267433. |
[33] | KEAM S J. Toripalimab:first global approval[J]. Drugs,2019,79(5):573-578. DOI:10.1007/s40265-019-01076-2. |
[34] | TANG B X,CHI Z H,CHEN Y B,et al. Safety,efficacy,and biomarker analysis of toripalimab in previously treated advanced melanoma:results of the POLARIS-01 multicenter phase II trial[J]. Clin Cancer Res,2020,26(16):4250-4259. DOI:10.1158/1078-0432.CCR-19-3922. |
[35] | WANG F H,WEI X L,FENG J F,et al. Efficacy,safety,and correlative biomarkers of toripalimab in previously treated recurrent or metastatic nasopharyngeal carcinoma:a phase II clinical trial (POLARIS-02)[J]. J Clin Oncol,2021,39(7):704-712. DOI:10.1200/JCO.20.02712. |
[36] | WANG F,WEI X L,WANG F H,et al. Safety,efficacy and tumor mutational burden as a biomarker of overall survival benefit in chemo-refractory gastric cancer treated with toripalimab,a PD-1 antibody in phase Ib/II clinical trial NCT02915432[J]. Ann Oncol,2019,30(9):1479-1486. DOI:10.1093/annonc/mdz197. |
[37] | LU M,ZHANG P P,ZHANG Y Q,et al. Efficacy,safety,and biomarkers of toripalimab in patients with recurrent or metastatic neuroendocrine neoplasms:a multiple-center phase ib trial[J]. Clin Cancer Res,2020,26(10):2337-2345. DOI:10.1158/1078-0432.CCR-19-4000. |
[38] | GAO S G,LI N,GAO S Y,et al. Neoadjuvant PD-1 inhibitor (Sintilimab) in NSCLC[J]. J Thorac Oncol,2020,15(5):816-826. DOI:10.1016/j.jtho.2020.01.017. |
[39] | ANSELL S M. Sintilimab:another effective immune checkpoint inhibitor in classical Hodgkin lymphoma[J]. Lancet Haematol,2019,6(1):e2-3. DOI:10.1016/S2352-3026(18)30210-2. |
[40] | YANG Y P,WANG Z H,FANG J,et al. Efficacy and safety of sintilimab plus pemetrexed and platinum as first-line treatment for locally advanced or metastatic nonsquamous NSCLC:a randomized,double-blind,phase 3 study (oncology pRogram by InnovENT anti-PD-1-11)[J]. J Thorac Oncol,2020,15(10):1636-1646. DOI:10.1016/j.jtho.2020.07.014. |
[41] | LAM V K,FORDE P M. Another brick in the wall:sintilimab plus chemotherapy in advanced lung cancer[J]. J Thorac Oncol,2020,15(10):1556-1558. DOI:10.1016/j.jtho.2020.08.013. |
[42] | LEE A,KEAM S J. Tislelizumab:first approval[J]. Drugs,2020,80(6):617-624. DOI:10.1007/s40265-020-01286-z. |
[43] | SONG Y Q,WU J Q,CHEN X C,et al. A single-arm,multicenter,phase II study of camrelizumab in relapsed or refractory classical Hodgkin lymphoma[J]. Clin Cancer Res,2019,25(24):7363-7369. DOI:10.1158/1078-0432.CCR-19-1680. |
[44] | QIN S,REN Z,MENG Z,et al. Camrelizumab in patients with previously treated advanced hepatocellular carcinoma:a multicentre,open-label,parallel-group,randomised,phase 2 trial[J]. Lancet Oncol,2020,21(4):571-580. DOI:10.1016/s1470-2045(20)30011-5. |
[45] | HUANG J,XU J M,CHEN Y,et al. Camrelizumab versus investigator's choice of chemotherapy as second-line therapy for advanced or metastatic oesophageal squamous cell carcinoma (ESCORT):a multicentre,randomised,open-label,phase 3 study[J]. Lancet Oncol,2020,21(6):832-842. DOI:10.1016/S1470-2045(20)30110-8. |
[46] | FAN Y,ZHAO J,WANG Q M,et al. Camrelizumab plus apatinib in extensive-stage SCLC (PASSION):a multicenter,two-stage,phase 2 trial[J]. J Thorac Oncol,2021,16(2):299-309. DOI:10.1016/j.jtho.2020.10.002. |
[47] | HERBST R S,SORIA J C,KOWANETZ M,et al. Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients[J]. Nature,2014,515(7528):563-567. DOI:10.1038/nature14011. |
[48] | APOLO A B,INFANTE J R,BALMANOUKIAN A,et al. Avelumab,an anti-programmed death-ligand 1 antibody,in patients with refractory metastatic urothelial carcinoma:results from a multicenter,phase ib study[J]. J Clin Oncol,2017,35(19):2117-2124. DOI:10.1200/JCO.2016.71.6795. |
[49] | GAISER M R,BONGIORNO M,BROWNELL I. PD-L1 inhibition with avelumab for metastatic Merkel cell carcinoma[J]. Expert Rev Clin Pharmacol,2018,11(4):345-359. DOI:10.1080/17512433.2018.1445966. |
[50] | GULLAPALLI S,REMON J,HENDRIKS L E L,et al. Update on targeted therapies for advanced non-small cell lung cancer:durvalumab in context[J]. Onco Targets Ther,2020,13:6885-6896. DOI:10.2147/OTT.S259308. |
[51] | STEWART R,MORROW M,HAMMOND S A,et al. Identification and characterization of MEDI4736,an antagonistic anti-PD-L1 monoclonal antibody[J]. Cancer Immunol Res,2015,3(9):1052-1062. DOI:10.1158/2326-6066.CIR-14-0191. |
[52] | GUZIK K,ZAK K M,GRUDNIK P,et al. Small-molecule inhibitors of the programmed cell death-1/programmed death-ligand 1 (PD-1/PD-L1) interaction via transiently induced protein states and dimerization of PD-L1[J]. J Med Chem,2017,60(13):5857-5867. DOI:10.1021/acs.jmedchem.7b00293. |
[53] | EGGERMONT A M M,KICINSKI M,BLANK C U,et al. Association between immune-related adverse events and recurrence-free survival among patients with stageⅢ melanoma randomized to receive pembrolizumab or placebo:a secondary analysis of a randomized clinical trial[J]. JAMA Oncol,2020,6(4):519-527. DOI:10.1001/jamaoncol.2019.5570. |
[54] | Squibb B-M. A Single-Arm,Open-Label,Multicenter Clinical Trial With Nivolumab (BMS-936558) for Subjects With Histologically Confirmed StageⅢ(Unresectable) or StageⅣMelanoma Progressing Post Prior Treatment Containing an Anti-CTLA4 Monoclonal Antibody (CheckMate 172). ,2014. |
[55] | MIGDEN M R,KHUSHALANI N I,CHANG A L S,et al.Cemiplimab in locally advanced cutaneous squamous cell carcinoma:results from an open-label,phase 2,single-arm trial[J]. Lancet Oncol,2020,21(2):294-305. DOI:10.1016/s1470-2045(19)30728-4. |
[56] | SHI Y K,SU H,SONG Y P,et al. Safety and activity of sintilimab in patients with relapsed or refractory classical Hodgkin lymphoma (ORIENT-1):a multicentre,single-arm,phase 2 trial[J]. Lancet Haematol,2019,6(1):e12-e19. DOI:10.1016/S2352-3026(18)30192-3. |
[57] | LAN C Y,SHEN J X,WANG Y,et al. Camrelizumab plus apatinib in patients with advanced cervical cancer (CLAP):a multicenter,open-label,single-arm,phase II trial[J]. J Clin Oncol,2020,38(34):4095-4106. DOI:10.1200/JCO.20.01920. |
[58] | Roche H-L. A Study of Atezolizumab in Participants With Locally Advanced or Metastatic Urothelial Bladder Cancer(Cohort 2,,2014. |
[59] | Astrazeneca. A Global Study to Assess the Effects of MEDI4736 Following Concurrent Chemoradiation in Patients With StageⅢUnresectable Non-Small Cell Lung Cancer. ,2014. |
[60] | KASTNER D L,AKSENTIJEVICH I,GOLDBACH-MANSKY R. Autoinflammatory disease reloaded:a clinical perspective[J]. Cell,2010,140(6):784-790. DOI:10.1016/j.cell.2010.03.002. |
[61] | BRAHMER J R,LACCHETTI C,THOMPSON J A. Management of immune-related adverse events in patients treated with immune checkpoint inhibitor therapy:American society of clinical oncology clinical practice guideline summary[J]. J Oncol Pract,2018,14(4):247-249. DOI:10.1200/JOP.18.00005. |
[62] | MALLETT G,LAURENCE A,AMARNATH S. Programmed cell death-1 receptor (PD-1)-mediated regulation of innate lymphoid cells[J]. Int J Mol Sci,2019,20(11):2836. DOI:10.3390/ijms20112836. |
[63] | MARIOTTI F R,QUATRINI L,MUNARI E,et al. Innate lymphoid cells:expression of PD-1 and other checkpoints in normal and pathological conditions[J]. Front Immunol,2019,10:910. DOI:10.3389/fimmu.2019.00910. |
[64] | TUMINO N,MARTINI S,MUNARI E,et al. Presence of innate lymphoid cells in pleural effusions of primary and metastatic tumors:Functional analysis and expression of PD-1 receptor[J]. Int J Cancer,2019,145(6):1660-1668. DOI:10.1002/ijc.32262. |
[65] | SCANVION Q,BÉNÉ J,GAUTIER S,et al. Moderate-to-severe eosinophilia induced by treatment with immune checkpoint inhibitors:37 cases from a national reference center for hypereosinophilic syndromes and the French pharmacovigilance database[J]. Oncoimmunology,2020,9(1):1722022. DOI:10.1080/2162402X.2020.1722022. |
[66] | CYBULSKA-STOPA B,KAMIZSKA-WINCIOREK G,DYDUCH G. Immune-related adverse events in a patient with eosinophilic enteritis treated with immune checkpoint inhibitors (anti-PD-1)[J]. Melanoma Res,2020,30(6):619-624. DOI:10.1097/CMR.0000000000000693. |
[67] | PENG Z,CHENG S Y,KOU Y,et al. The gut microbiome is associated with clinical response to anti-PD-1/PD-L1 immunotherapy in gastrointestinal cancer[J]. Cancer Immunol Res,2020,8(10):1251-1261. DOI:10.1158/2326-6066.CIR-19-1014. |
[68] | ROUTY B,LE CHATELIER E,DEROSA L,et al. Gut microbiome influences efficacy of PD-1-based immunotherapy against epithelial tumors[J]. Science,2018,359(6371):91-97. DOI:10.1126/science.aan3706. |
[69] | GOPALAKRISHNAN V,SPENCER C N,NEZI L,et al. Gut microbiome modulates response to anti-PD-1 immunotherapy in melanoma patients[J]. Science,2018,359(6371):97-103. |
[70] | OH D Y,CHAM J,ZHANG L,et al. Immune toxicities elicted by CTLA-4 blockade in cancer patients are associated with early diversification of the T-cell repertoire[J]. Cancer Res,2017,77(6):1322-1330. DOI:10.1158/0008-5472.CAN-16-2324. |
[71] | LIBERT C,DEJAGER L. How steroids steer T cells[J]. Cell Rep,2014,7(4):938-939. DOI:10.1016/j.celrep.2014.04.041. |
[72] | LINSLEY P S,BRADY W,URNES M,et al. CTLA-4 is a second receptor for the B cell activation antigen B7[J]. J Exp Med,1991,174(3):561-569. DOI:10.1084/jem.174.3.561. |
[73] | XU-MONETTE Z Y,ZHOU J F,YOUNG K H. PD-1 expression and clinical PD-1 blockade in B-cell lymphomas[J]. Blood,2018,131(1):68-83. DOI:10.1182/blood-2017-07-740993. |
[74] | DAS R,BAR N,FERREIRA M,et al. Early B cell changes predict autoimmunity following combination immune checkpoint blockade[J]. J Clin Invest,2018,128(2):715-720. DOI:10.1172/JCI96798. |
[75] | ESFAHANI K,ELKRIEF A,CALABRESE C,et al. Moving towards personalized treatments of immune-related adverse events[J]. Nat Rev Clin Oncol,2020,17(8):504-515. DOI:10.1038/s41571-020-0352-8. |
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