Efficacy and peripheral immunity analysis of allogeneic natural killer cells therapy in patients with hepatocellular carcinoma

  • Yun-bo XIE ,
  • Ji-yuan ZHANG ,
  • Mei-ling DU ,
  • Fan-ping MENG ,
  • Jun-liang FU ,
  • Li-min LIU ,
  • Song-shan WANG ,
  • Rui QU ,
  • Fang LIAN ,
  • Fei QIAO ,
  • Yang-liu CHEN ,
  • Ying-ying GAO ,
  • Ruo-nan XU ,
  • Ming SHI ,
  • Fu-sheng WANG
Expand
  • Institute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China

Received date: 2019-03-18

  Online published: 2019-06-26

Supported by

Supported by the National Natural Science Foundation of China(81721002,81571567)

Abstract

Objective: To evaluate the safety and efficacy of allogeneic natural killer (NK) cells in the treatment of primary hepatocellular carcinoma (HCC), and to elucidate the mechanism of NK cells therapy.Methods: Twenty-one patients with primary HCC treated with allogeneic NK cells at the Fifth Medical Center of the PLA General Hospital were followed up for 1 year. Peripheral blood mononuclear cells (PBMCs) were isolated from patient-related donors and cultured in vitro for 15 days and infused to the patients in two consecutive days. Clinical data and laboratory data were collected and analyzed, including survival, clinical features, imaging changes, hematology, immunology, and biochemical indicators to evaluate the safety and efficacy of allogeneic NK cell therapy. The changes of peripheral blood lymphocyte subsets after treatment were also analyzed to explore the possible anti-tumor mechanisms. Results: (1) Of the 21 patients with primary HCC, 11 patients were treated once, 5 patients were treated twice, and 5 patients were treated 3 times. After allogeneic NK cells infusion, 10 patients had fever, 1 patient had slight hepatalgia and 1 patient had slight headache, no other adverse events occurred including acute and chronic graft-versus-host disease (GVHD). They resolved spontaneously within 8 hours without other treatment. (2) The total disease control rate was 76.2% during one-year follow-up. Among them, the patients with Barcelona clinic liver cancer (BCLC) stage A had a disease control rate of 100%, stable disease (SD) in 10 cases; BCLC stage B patients had a disease control rate of 60%, partial response (PR) in 1 case, and SD 2 in cases; BCLC stage C patients had a disease control rate of 50%, complete response (CR) in 1 case, and 2 cases of PR. (3) The frequencies of NK cells and CD8+ T cells in peripheral blood were significantly lower than that before at 24 hours after treatment, and the frequencies of CD4+ T cells and CD4/CD8 were significantly higher than the baseline.Conclusion: Allogeneic NK cells have good safety and efficacy in the treatment of primary HCC. The anti-tumor effect of the allogeneic NK cells may play an important role in the activation of the patient’s natural immune system and delay disease progression, suggesting that allogeneic NK cells combined with sorafenib may be a very effective treatment for advanced HCC, and further large-sample multicenter randomized controlled clinical trials are needed to validate this result.

Cite this article

Yun-bo XIE , Ji-yuan ZHANG , Mei-ling DU , Fan-ping MENG , Jun-liang FU , Li-min LIU , Song-shan WANG , Rui QU , Fang LIAN , Fei QIAO , Yang-liu CHEN , Ying-ying GAO , Ruo-nan XU , Ming SHI , Fu-sheng WANG . Efficacy and peripheral immunity analysis of allogeneic natural killer cells therapy in patients with hepatocellular carcinoma[J]. Journal of Peking University(Health Sciences), 2019 , 51(3) : 591 -595 . DOI: 10.19723/j.issn.1671-167X.2019.03.032

References

[1] Boni C, Lampertico P, Talamona L , et al. Natural killer cell phenotype modulation and natural killer/T-cell interplay in nucleos(t)ide analogue-treated hepatitis e antigen-negative patients with chronic hepatitis B[J]. Hepatology, 2015,62(6):1697-1709.
[2] Cai L, Zhang Z, Zhou L , et al. Functional impairment in circulating and intrahepatic NK cells and relative mechanism in hepatocellular carcinoma patients[J]. Clin Immunol, 2008,129(3):428-437.
[3] Easom NJW, Stegmann KA, Swadling L , et al. IL-15 overcomes hepatocellular carcinoma-induced NK cell dysfunction[J]. Front Immunol, 2018,9:1009.
[4] Liu P, Chen L, Zhang H. Natural killer cells in liver disease and hepatocellular carcinoma and the NK cell-based immunotherapy [J/OL]. J Immunol Res, 2018, 2018: 1206737.( 2018-09-04)[2019-03-01].https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142725/ .
[5] Parkhurst MR, Riley JP, Dudley ME , et al. Adoptive transfer of autologous natural killer cells leads to high levels of circulating natural killer cells but does not mediate tumor regression[J]. Clin Cancer Res, 2011,17(19):6287-6297.
[6] Guillerey C, Huntington ND, Smyth MJ . Targeting natural killer cells in cancer immunotherapy[J]. Nat Immunol, 2016,17(9):1025-1036.
[7] Eisenhauer EA, Therasse P, Bogaerts J , et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1)[J]. Eur J Cancer, 2009,45(2):228-247.
[8] Wong PPC, Kariminia A, Jones D , et al. Plerixafor effectively mobilizes CD56 (bright) NK cells in blood, providing an allograft predicted to protect against GVHD[J]. Blood, 2018,131(25):2863-2866.
[9] Ullrich E, Salzmann-Manrique E, Bakhtiar S , et al. Relation between acute GVHD and NK cell subset reconstitution following allogeneic stem cell transplantation[J]. Front Immunol, 2016,7:595.
[10] Kariminia A, Ivison S, Ng B , et al. CD56 (bright) natural killer regulatory cells in filgrastim primed donor blood or marrow products regulate chronic graft-versus-host disease: the Canadian Blood and Marrow Transplant Group randomized 0601 study results[J]. Haematologica, 2017,102(11):1936-1946.
[11] Qin Z, Chen J, Zeng J , et al. Effect of NK cell immunotherapy on immune function in patients with hepatic carcinoma: a preliminary clinical study[J]. Cancer Biol Ther, 2017,18(5):323-330.
[12] Miller JS, Soignier Y, Panoskaltsis-Mortari A , et al. Successful adoptive transfer and in vivo expansion of human haploidentical NK cells in patients with cancer[J]. Blood, 2005,105(8):3051-3057.
[13] Llovet JM, Ricci S, Mazzaferro V , et al. Sorafenib in advanced hepatocellular carcinoma[J]. N Engl J Med, 2008,359(4):378-390.
[14] Kohga K, Takehara T, Tatsumi T , et al. Sorafenib inhibits the shedding of major histocompatibility complex class Ⅰ-related chain A on hepatocellular carcinoma cells by down-regulating a disintegrin and metalloproteinase 9[J]. Hepatology, 2010,51(4):1264-1273.
[15] Sprinzl MF, Reisinger F, Puschnik A , et al. Sorafenib perpetuates cellular anticancer effector functions by modulating the crosstalk between macrophages and natural killer cells[J]. Hepatology, 2013,57(6):2358-2368.
Outlines

/