Aronthippaitoon Yada, Szerman Nathan, Ngo-Giang-Huong Nicole, Laperche Syria, Ungeheuer Marie-Noelle, Sureau Camille, Khamduang Woottichai, Gaudy-Graffin Catherine
Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50100, Thailand.
LUCENT International Collaboration, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50100, Thailand.
Vaccines (Basel). 2023 Apr 4;11(4):791. doi: 10.3390/vaccines11040791.
Anti-HBs antibodies are elicited upon hepatitis B vaccination, and concentrations above 10 mIU/mL are considered protective. Our aim was to assess the relationship between IU/mL of anti-HBs and neutralization activity.
Immunoglobulins G (IgGs) were purified from individuals who received a serum-derived vaccine (Group 1), a recombinant vaccine, Genevac-B or Engerix-B (Group 2), or who recovered from acute infection (Group 3). IgGs were tested for anti-HBs, anti-preS1, and anti-preS2 antibodies and for their neutralizing activity in an in vitro infection assay.
Anti-HBs IUs/mL value did not strictly correlate with neutralization activity. The Group 1 antibodies demonstrated a greater neutralizing activity than those of Group 2. Anti-preS1 antibodies were detected in Groups 1 and 3, and anti-preS2 in Group 1 and Group 2/Genhevac-B, but the contribution of anti-preS antibodies to neutralization could not be demonstrated. Virions bearing immune escape HBsAg variants were less susceptible to neutralization than wild-type virions.
The level of anti-HBs antibodies in IUs is not sufficient to assess neutralizing activity. Consequently, (i) an in vitro neutralization assay should be included in the quality control procedures of antibody preparations intended for HB prophylaxis or immunotherapy, and (ii) a greater emphasis should be placed on ensuring that vaccine genotype/subtype matches with that of the circulating HBV.
乙肝疫苗接种后可产生抗-HBs抗体,浓度高于10 mIU/mL被认为具有保护作用。我们的目的是评估抗-HBs的IU/mL与中和活性之间的关系。
从接受血清源性疫苗(第1组)、重组疫苗(Genevac-B或Engerix-B,第2组)或从急性感染中康复的个体(第3组)中纯化免疫球蛋白G(IgG)。检测IgG的抗-HBs、抗-preS1和抗-preS2抗体,并在体外感染试验中检测其中和活性。
抗-HBs的IU/mL值与中和活性并不严格相关。第1组抗体的中和活性高于第2组。在第1组和第3组中检测到抗-preS1抗体,在第1组和第2组/Genhevac-B中检测到抗-preS2抗体,但无法证明抗-preS抗体对中和作用的贡献。携带免疫逃逸HBsAg变异体的病毒颗粒比野生型病毒颗粒更不易被中和。
以IU为单位的抗-HBs抗体水平不足以评估中和活性。因此,(i)在用于乙肝预防或免疫治疗的抗体制剂的质量控制程序中应包括体外中和试验,(ii)应更加重视确保疫苗基因型/亚型与流行的乙肝病毒基因型/亚型相匹配。