Evidence map›Paper›PMID 42188755›Full record

ArticleVaccines2026

Impact of Media and Induction Strategy on Physicochemical Characteristics and Immunogenicity of Recombinant fHbp-PorA Chimeric Protein: A Promising Meningococcal B Vaccine Candidate Produced in

Annamraju Aswini, Annamraju D Sarma, Ashish B Deshpande, Yogesh C Padwal, Vinay V Gavade, Sambhaji S Pisal, Selvan Ravindran

Abstract read
In one paragraph

Article in Vaccines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Annamraju AswiniSerum Institute of India Pvt. Ltd., Hadapsar, Pune 411028, India.ORCID 0009-0007-7098-8375
Annamraju D SarmaSerum Institute of India Pvt. Ltd., Hadapsar, Pune 411028, India.
Ashish B DeshpandeSerum Institute of India Pvt. Ltd., Hadapsar, Pune 411028, India.ORCID 0000-0001-9723-0045
Yogesh C PadwalSerum Institute of India Pvt. Ltd., Hadapsar, Pune 411028, India.
Vinay V GavadeSerum Institute of India Pvt. Ltd., Hadapsar, Pune 411028, India.ORCID 0009-0000-4132-953X
Sambhaji S PisalSerum Institute of India Pvt. Ltd., Hadapsar, Pune 411028, India.
Selvan RavindranSymbiosis School of Biological Sciences (SSBS), Faculty of Medical and Health Sciences, Symbiosis International (Deemed University), Lavale, Pune 412115, India.ORCID 0000-0001-6846-319X

Funding

Serum Institute of India Pvt. Ltd
6 · The paper itself

Abstract

BACKGROUND/

objectiveApart from the attributes such as cost, yields and consistency that define the feasibility of a manufacturing process, physicochemical and immunological quality traits equally signify the functionality of a biological product. The present study investigates one such promising Meningococcal B vaccine candidate, a chimeric fHbp-PorA protein in

resultsGrowth in the CD media resulted in several-fold-higher biomass compared to that in CM media in a short cultivation time; however, more than a third of the expressed protein remained in an insoluble state. Meanwhile, almost all of the expressed protein with CM media was recovered in soluble form. Moreover, purification of the unprocessed tagged protein and recovery of chimeric protein (tag removed) resulted in 75% greater yield in CM media when compared to CD media. The final chimeric proteins obtained from each medium varied significantly in their physicochemical characteristics, including their epitope projection and CD spectra. The results of

conclusionsThe outcomes demonstrate that complex media with galactose-induced expression not only show higher productivity but also exhibit superior quality attributes, qualifying their reliable use in the manufacturing process of this promising vaccine candidate.

Indexed as

Escherichia colifHbp-PorAimmunogenicityinduction strategymedia optimizationMeningococcal B chimeric proteinrecombinant vaccine

Identifiers

PMID42188755
PMCPMC13211582

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.