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COVID-19 mRNA 疫苗在患有淋巴恶性肿瘤或抗 CD20 抗体治疗的患者中的应用:一项系统评价和荟萃分析。

COVID-19 mRNA Vaccine in Patients With Lymphoid Malignancy or Anti-CD20 Antibody Therapy: A Systematic Review and Meta-Analysis.

机构信息

Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

出版信息

Clin Lymphoma Myeloma Leuk. 2022 Aug;22(8):e691-e707. doi: 10.1016/j.clml.2022.03.012. Epub 2022 Mar 28.

Abstract

BACKGROUND

The humoral response to vaccination in individuals with lymphoid malignancies or those undergoing anti-CD20 antibody therapy is impaired, but details of the response to mRNA vaccines to protect against COVID-19 remain unclear. This systematic review and meta-analysis aimed to characterize the response to COVID-19 mRNA vaccines in patients with lymphoid malignancies or those undergoing anti-CD20 antibody therapy.

MATERIALS AND METHODS

A literature search retrieved 52 relevant articles, and random-effect models were used to analyze humoral and cellular responses.

RESULTS

Lymphoid malignancies and anti-CD20 antibody therapy for non-malignancies were significantly associated with lower seropositivity rates (risk ratio 0.60 [95% CI 0.53-0.69]; risk ratio 0.45 [95% CI 0.39-0.52], respectively). Some subtypes (chronic lymphocytic leukemia, treatment-naïve chronic lymphocytic leukemia, myeloma, and non-Hodgkin's lymphoma) exhibited impaired humoral response. Anti-CD20 antibody therapy within 6 months of vaccination decreased humoral response; moreover, therapy > 12 months before vaccination still impaired the humoral response. However, anti-CD20 antibody therapy in non-malignant patients did not attenuate T cell responses.

CONCLUSION

These data suggest that patients with lymphoid malignancies or those undergoing anti-CD20 antibody therapy experience an impaired humoral response, but cellular response can be detected independent of anti-CD20 antibody therapy. Studies with long-term follow-up of vaccine effectiveness are warranted (PROSPERO registration number: CRD42021265780).

摘要

背景

患有淋巴恶性肿瘤或正在接受抗 CD20 抗体治疗的个体对疫苗的体液反应受损,但针对预防 COVID-19 的 mRNA 疫苗的反应细节仍不清楚。本系统评价和荟萃分析旨在描述淋巴恶性肿瘤患者或正在接受抗 CD20 抗体治疗的患者对 COVID-19 mRNA 疫苗的反应。

材料和方法

文献检索检索到 52 篇相关文章,并使用随机效应模型分析体液和细胞反应。

结果

淋巴恶性肿瘤和非恶性疾病的抗 CD20 抗体治疗与较低的血清阳性率显著相关(风险比 0.60[95%CI0.53-0.69];风险比 0.45[95%CI0.39-0.52])。一些亚型(慢性淋巴细胞白血病、初治慢性淋巴细胞白血病、骨髓瘤和非霍奇金淋巴瘤)表现出受损的体液反应。疫苗接种前 6 个月内的抗 CD20 抗体治疗降低了体液反应;此外,疫苗接种前 12 个月以上的治疗仍会损害体液反应。然而,非恶性疾病患者的抗 CD20 抗体治疗不会减弱 T 细胞反应。

结论

这些数据表明,患有淋巴恶性肿瘤或正在接受抗 CD20 抗体治疗的患者会出现受损的体液反应,但可以检测到独立于抗 CD20 抗体治疗的细胞反应。需要进行长期随访疫苗有效性的研究(PROSPERO 注册号:CRD42021265780)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca9c/8958822/a9f91a84858d/gr1_lrg.jpg

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