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Immunogenicity and safety of subunit influenza vaccines in pregnant women

机译:孕妇亚单位流感疫苗的免疫原性和安全性

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Pregnancy is a condition of modulated immune suppression, so this group of patients has increased risk of infectious diseases.Trivalent subunit vaccines, unadjusted Agrippal S1 (group I) and immunoadjuvant Grippol Plus (group II), containing 5?μg of actual influenza virus strains, were administered respectively to 37 and 42 women in the second and third trimester of physiological pregnancy.The administration of subunit influenza vaccines was accompanied by the development of local reactions in no more than 10% of patients, compared with 4.9% of the 41 pregnant women in the placebo group (group III). Systemic reactions were of a general somatic nature, did not differ between vaccinated and placebo groups, and were not associated with vaccination. Physiological births in groups I, II and III were 94.6%, 92.9% and 85.4%, respectively, and the birth rates of children without pathologies were 91.9%, 90.5% and 80.5%, respectively, and were comparable between groups. Vaccination stimulated the production of protective antibodies against influenza virus strains in 64.8–94.5% of patients after immunisation with an unadjusted vaccine and in 72.5–90.0% of patients after the administration of an immunoadjuvant vaccine. After 9?months, antibody levels were recorded in 51.3–72.9% in group I and 54.2–74.2% in group II. Immunisation against influenza in pregnant women provided a high level of seroprotection and seroconversion. Nevertheless, the level of seroprotection against the influenza strain A(H3N2, Victoria) was slightly lower in the group immunised with an unadjusted vaccine compared to those vaccinated with the immunoadjuvant vaccine.The trivalent subunit anti-influenza vaccines Agrippal S1 and Grippol Plus are an effective means of preventing influenza for pregnant women http://ow.ly/fCJS30iFvfz
机译:怀孕是调节性免疫抑制的条件,因此该组患者增加了感染疾病的风险。三价亚单位疫苗,未经调整的Agrippal S1(I组)和免疫佐剂Grippol Plus(II组),含有5μg实际流感病毒株分别在生理学妊娠的中期和中期向37和42名妇女进行了接种,亚单位流感疫苗的接种伴随局部反应的发生率不超过10%,而41名孕妇中只有4.9%安慰剂组中的女性(第三组)。全身反应具有一般的躯体性质,在接种疫苗组和安慰剂组之间没有区别,并且与疫苗接种无关。 I,II和III组的生理学出生率分别为94.6%,92.9%和85.4%,无病儿童的出生率分别为91.9%,90.5%和80.5%,两组之间具有可比性。接种疫苗后,未经调整的疫苗免疫后,在64.8–94.5%的患者中刺激产生针对流感病毒株的保护性抗体,而在免疫佐剂疫苗接种后,在72.5–90.0%的患者中刺激了针对流感病毒株的保护性抗体的产生。 9个月后,I组的抗体水平记录为51.3–72.9%,II组的抗体水平记录为54.2–74.2%。孕妇的流感疫苗接种提供了高水平的血清保护和血清转化。然而,与未接种免疫佐剂疫苗的人群相比,未经调整疫苗接种的人群对A型流感病毒(H3N2,Victoria)的血清保护水平略低。三价亚单位抗流感疫苗Agrippal S1和Grippol Plus是一种预防孕妇流感的有效方法

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