Neutralizing SARS-CoV-2 Antibodies in Commercial Immunoglobulin Products Give Patients with X-Linked Agammaglobulinemia Limited Passive Immunity to the Omicron Variant

被引:16
作者
Lindahl, Hannes [1 ,2 ]
Klingstrom, Jonas [3 ]
Da Silva Rodrigues, Rui [1 ]
Christ, Wanda [3 ]
Chen, Puran [3 ]
Ljunggren, Hans-Gustaf [3 ]
Buggert, Marcus [3 ]
Aleman, Soo [3 ,4 ]
Smith, C. I. Edvard [4 ,5 ]
Bergman, Peter [4 ,5 ]
机构
[1] Karolinska Univ Hosp, Dept Clin Immunol & Transfus Med, Stockholm, Sweden
[2] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[3] Karolinska Inst, Dept Med Huddinge, Stockholm, Sweden
[4] Karolinska Univ Hosp, Dept Infect Dis, Stockholm, Sweden
[5] Karolinska Inst, Dept Lab Med, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Primary immunodeficiency; Immunoglobulin replacement therapy; SARS-CoV-2; Omicron; Passive immunity; X-linked agammaglobulinemia;
D O I
10.1007/s10875-022-01283-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunodeficient individuals often rely on donor-derived immunoglobulin (Ig) replacement therapy (IGRT) to prevent infections. The passive immunity obtained by IGRT is limited and reflects the state of immunity in the plasma donor population at the time of donation. The objective of the current study was to describe how the potential of passive immunity to SARS-CoV-2 in commercial off-the-shelf Ig products used for IGRT has evolved during the pandemic. Samples were collected from all consecutive Ig batches (n = 60) from three Ig producers used at the Immunodeficiency Unit at Karolinska University Hospital from the start of the SARS-CoV-2 pandemic until January 2022. SARS-CoV-2 antibody concentrations and neutralizing capacity were assessed in all samples. In vivo relevance was assessed by sampling patients with XLA (n = 4), lacking endogenous immunoglobulin synthesis and on continuous Ig substitution, for plasma SARS-CoV-2 antibody concentration. SARS-CoV-2 antibody concentrations in commercial Ig products increased over time but remained inconsistently present. Moreover, Ig batches with high neutralizing capacity towards the Wuhan-strain of SARS-CoV-2 had 32-fold lower activity against the Omicron variant. Despite increasing SARS-CoV-2 antibody concentrations in commercial Ig products, four XLA patients on IGRT had relatively low plasma concentrations of SARS-CoV-2 antibodies with no potential to neutralize the Omicron variant in vitro. In line with this observation, three out the four XLA patients had symptomatic COVID-19 during the Omicron wave. In conclusion, 2 years into the pandemic the amounts of antibodies to SARS-CoV-2 vary considerably among commercial Ig batches obtained from three commercial producers. Importantly, in batches with high concentrations of antibodies directed against the original virus strain, protective passive immunity to the Omicron variant appears to be insufficient.
引用
收藏
页码:1130 / 1136
页数:7
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