Kreitman Robert J, James Lacey, Feurtado Julie, Eager Holly, Sierra Ortiz Olena, Gould Mory, Shpilman Isaac, Zhou Hong, Burbelo Peter D, Cohen Jeffrey I, Wang Hao-Wei, Yuan Constance M, Arons Evgeny
Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Office of Research Nursing, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Blood Neoplasia. 2024 Aug 28;1(4):100035. doi: 10.1016/j.bneo.2024.100035. eCollection 2024 Dec.
Patients with the B-cell malignancy hairy cell leukemia (HCL) and the poorer-prognosis variant HCLv often receive anti-CD20 monoclonal antibodies (mAbs), which kill normal B cells, impairing humoral immunity. We measured COVID-19 antibodies after doses of COVID-19 vaccine in patients with HCL (n = 415) and HCLv (n = 32). After the second COVID-19 vaccine dose, spike antibody level most strongly correlated with normal B-cell levels (r = 0.365, < .0001), followed by CD4 T-cell count (r = 0.244, = .0002), and was less related to immunoglobulin G level (r = 0.101, = .14). Spike antibody also correlated with normal B cells after the third to fifth vaccine doses and with CD4 count after the third dose. Normal B-cells were undetectable in 87% of patients within 6 months after the last dose of anti-CD20 mAb and were lower than in patients at 6 to 12 months ( = .0003), which, in turn, were lower than at 12 to 18 months ( = .0002). Infection with COVID-19 became more common after use of the third vaccine dose; spike antibody levels were higher in patients with prior infection (positive vs negative nucleocapsid antibodies; < .0001). Spike antibodies decreased faster after ibrutinib or anti-CD20 mAb. We conclude that decreased levels of normal B cells in patients with HCL/HCLv, due to disease and/or anti-CD20 therapy, are associated with lower COVID-19 vaccination efficiency and such patients may not respond well to vaccines. The associated studies were registered at www.ClinicalTrials.gov as #NCT01087333 (HCL/HCLv) and #NCT04362865 (COVID-19).
患有B细胞恶性肿瘤毛细胞白血病(HCL)和预后较差的变异型HCLv(HCLv)的患者经常接受抗CD20单克隆抗体(mAb)治疗,这些抗体会杀死正常B细胞,损害体液免疫。我们测量了HCL患者(n = 415)和HCLv患者(n = 32)接种COVID-19疫苗后的抗体情况。在接种第二剂COVID-19疫苗后,刺突抗体水平与正常B细胞水平的相关性最强(r = 0.365,P <.0001),其次是CD4 T细胞计数(r = 0.244,P =.0002),与免疫球蛋白G水平的相关性较小(r = 0.101,P =.14)。在接种第三至第五剂疫苗后,刺突抗体也与正常B细胞相关,在接种第三剂疫苗后与CD4计数相关。在最后一剂抗CD20 mAb治疗后的6个月内,87%的患者检测不到正常B细胞,且其水平低于6至12个月的患者(P =.0003),而6至12个月的患者又低于12至18个月的患者(P =.0002)。在接种第三剂疫苗后,COVID-19感染变得更加常见;既往感染患者的刺突抗体水平更高(核衣壳抗体阳性与阴性;P <.0001)。在使用伊布替尼或抗CD20 mAb后,刺突抗体下降得更快。我们得出结论,由于疾病和/或抗CD20治疗,HCL/HCLv患者的正常B细胞水平降低与COVID-19疫苗接种效率较低有关,此类患者可能对疫苗反应不佳。相关研究已在www.ClinicalTrials.gov上注册,注册号为#NCT01087333(HCL/HCLv)和#NCT04362865(COVID-19)。