National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, Georgia 30341, United States.
Seqirus, a CSL Company, 50 Hampshire Street, Cambridge, Massachusetts 02139, United States.
Anal Chem. 2020 Sep 1;92(17):11879-11887. doi: 10.1021/acs.analchem.0c02252. Epub 2020 Aug 12.
Avian influenza viruses, such as A(H5N1) and A(H7N9), are primary public health concerns due to their pandemic potential. Influenza vaccines represent the most effective response to this threat especially with timely provision. The current pandemic response timelines require a substantial period for strain-specific reference antigen and sera preparation for use with single-radial immunodiffusion (SRID), the accepted vaccine potency assay. To address this time lag, the isotope dilution mass spectrometry (IDMS) method was developed to quantify the absolute hemagglutinin (HA, the main influenza antigen) amount in the vaccine without the need for purified, inactivated, and calibrated virus reference antigens. However, an additional challenge in determining potency is to differentiate between vaccine antigens in their most potent form from other less potent, stressed antigen forms. The limited trypsin digestion (LTD) method has been developed and does not require strain-specific full-length reference antigens or antibodies; instead, stressed HA is selectively degraded, leaving the more potent form to be measured. LTD, followed by precipitation and IDMS, allows for efficient differentiation between potent and significantly less potent HA for vaccine release and potency testing across the vaccine's shelf life. In this study, we tested the LTD-IDMS assay on A(H5N1) vaccine material that had been stressed by low pH, heat, and multiple freeze-thaw cycles. The results showed that the LTD-IDMS method effectively quantified the potent HA in A(H5N1) vaccine material with results comparable to SRID. As such, it shows great promise to complement and potentially replace SRID in a pandemic when strain-specific reagents may not be readily available.
禽流感病毒,如 A(H5N1)和 A(H7N9),因其大流行的潜力而成为主要的公共卫生关注点。流感疫苗是应对这一威胁的最有效手段,尤其是在及时提供的情况下。目前的大流行应对时间表要求在特定菌株的参考抗原和血清制备方面需要相当长的时间,以便与单放射免疫扩散(SRID)一起使用,SRID 是公认的疫苗效力检测方法。为了解决这个时间滞后问题,开发了同位素稀释质谱法(IDMS)来定量疫苗中绝对血凝素(HA,主要的流感抗原)的含量,而无需使用纯化、灭活和校准的病毒参考抗原。然而,在确定效力方面的另一个挑战是区分疫苗抗原的最有效形式与其他效力较低、应激的抗原形式。已经开发了有限胰蛋白酶消化(LTD)方法,该方法不需要特定菌株的全长参考抗原或抗体;相反,应激的 HA 会被选择性降解,留下更有效的形式进行测量。LTD 随后进行沉淀和 IDMS,可以有效地区分疫苗在其保质期内释放和效力测试中效力较高和显著较低的 HA。在这项研究中,我们对经过低 pH 值、热和多次冻融循环应激的 A(H5N1)疫苗材料进行了 LTD-IDMS 检测。结果表明,LTD-IDMS 方法能够有效地定量 A(H5N1)疫苗材料中的有效 HA,其结果与 SRID 相当。因此,当特定菌株的试剂可能不容易获得时,它有望在大流行期间补充并可能替代 SRID。