Goldwater Marissa-Skye, Stampfer Samuel D, Sean Regidor Bernard, Bujarski Sean, Jew Scott, Chen Haiming, Xu Ning, Kim Clara, Kim Susanna, Berenson James R
Institute for Myeloma and Bone Cancer Research, West Hollywood, CA, United States.
Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA, United States.
Clin Infect Pract. 2023 Jan;17:100214. doi: 10.1016/j.clinpr.2022.100214. Epub 2022 Dec 13.
We have reported that IgG antibody responses following two mRNA COVID-19 vaccinations are impaired among patients with multiple myeloma (MM). In the current study, sixty-seven patients with MM were tested for anti-spike IgG antibodies 0-60 days prior to their first vaccination, 14-28 days following the second dose, and both before and 14-28 days after their third dose of the mRNA-1273 or BNT162b2 vaccines. After the first two doses, most patients' (93 %) antibody levels declined to ineffective levels (<250 BAU/mL) prior to their third dose (D3). D3 elicited responses in 84 % of patients (61 % full response and 22 % partial response). The third vaccination increased antibody levels (average = 370.4 BAU/mL; range, 1.0-8977.3 BAU/mL) relative to just prior to D3 (average = 25.0 BAU/mL; range, 1.0-683.8 BAU/mL) and achieved higher levels than peak levels after the first two doses (average = 144.8 BAU/mL; range, 1.0-4,284.1 BAU/mL). D3 response positively correlated with mRNA-1273, a > 10-fold change from baseline for the two-dose series, switching from BNT162b2 to mRNA-1273 for D3, and treatment with elotuzumab and an immunomodulatory agent. Lower antibody levels prior to D3, poorer overall response to first two doses, and ruxolitinib or anti-CD38 monoclonal antibody treatment negatively correlated with D3 response. Our results show encouraging activity of the third vaccine, even among patients who failed to respond to the first two vaccinations. The finding of specific factors that predict COVID-19 antibody levels will help advise patients and healthcare professionals on the likelihood of responses to further vaccinations.
我们曾报道,多发性骨髓瘤(MM)患者在接种两剂mRNA新冠疫苗后的IgG抗体反应受损。在当前研究中,对67例MM患者在首次接种前0至60天、第二剂接种后14至28天以及第三剂mRNA-1273或BNT162b2疫苗接种前和接种后14至28天检测抗刺突IgG抗体。在前两剂接种后,大多数患者(93%)在第三剂(D3)接种前抗体水平降至无效水平(<250 BAU/mL)。D3在84%的患者中引发反应(61%完全反应和22%部分反应)。相对于D3前(平均=25.0 BAU/mL;范围1.0至683.8 BAU/mL),第三剂疫苗接种使抗体水平升高(平均=370.4 BAU/mL;范围1.0至8977.3 BAU/mL),且高于前两剂接种后的峰值水平(平均=144.8 BAU/mL;范围1.0至4284.1 BAU/mL)。D3反应与mRNA-1273、两剂系列相对于基线变化>10倍、D3从BNT162b2换用mRNA-1273以及使用埃罗妥珠单抗和免疫调节剂治疗呈正相关。D3前抗体水平较低、对前两剂总体反应较差以及使用芦可替尼或抗CD38单克隆抗体治疗与D3反应呈负相关。我们的结果显示第三剂疫苗具有令人鼓舞的活性,即使在对前两剂接种无反应的患者中也是如此。确定预测新冠抗体水平的特定因素这一发现将有助于为患者和医护人员提供关于进一步接种疫苗反应可能性的建议。