Evidence map›Paper›PMID 42807280›Full record

ArticleFrontiers in pediatrics2026

Developing affordable monoclonal antibodies for LMICs through high performance manufacturing processes and LMIC based commercial manufacturing.

Greg Pennypacker, Yetunde Adewunmi, Hannah Lichtenberger, Diana Herrin, Mary Jean Guillermo, Enrique Cowen, Leigh Pierce, Greg Hanson, Giovanna Chiyoko Weinman, Grace Richardson and 5 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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

15 authors.

Greg PennypackerServareGMP, San Diego, CA, United States.
Yetunde AdewunmiWadsworth-Laboratory of Microbial Pathogenesis and Immunology (MPI) Division of Infectious Diseases, Wadsworth Center, Albany, NY, United States.
Hannah LichtenbergerServareGMP, San Diego, CA, United States.
Diana HerrinServareGMP, San Diego, CA, United States.
Mary Jean GuillermoServareGMP, San Diego, CA, United States.
Enrique CowenServareGMP, San Diego, CA, United States.
Leigh PierceServareGMP, San Diego, CA, United States.
Greg HansonServareGMP, San Diego, CA, United States.
Giovanna Chiyoko WeinmanServareGMP, San Diego, CA, United States.
Grace RichardsonServareGMP, San Diego, CA, United States.
Yosef AlemiServareGMP, San Diego, CA, United States.
Nicholas J MantisWadsworth-Laboratory of Microbial Pathogenesis and Immunology (MPI) Division of Infectious Diseases, Wadsworth Center, Albany, NY, United States.
Tsepo Lebiletsa TsekoaCSIR-Biomanufacturing, Council for Scientific and Industrial Research, Pretoria, South Africa.
Rachel ChikwambaCSIR-Biomanufacturing, Council for Scientific and Industrial Research, Pretoria, South Africa.
Gary PierceServareGMP, San Diego, CA, United States.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Monoclonal Antibodies (mAbs) are one of the most effective developments in disease prevention and treatment of the last century. Active treatment and passive immunization with mAbs targeting key antigens represents a promising approach to preventing and mitigating infectious pathogen-caused illness, particularly in Low and Middle-Income Countries (LMICs). While the development of mAbs against infectious disease has lagged behind that of immune disorders and oncology targets, recent efforts against infectious diseases have seen increasing focus with the development of mAbs against RSV, Ebola strains, and SARS-CoV-2, among others. The price for mAb treatment remains out of reach for most patients in middle income countries and nearly all patients in low-income countries. It is therefore clear that a new approach to manufacturing mAbs is needed. Here, high-productivity, high-yield mAb fed-batch production is demonstrated using clonal variants of ZAC-3, a mAb directed against the conserved core/lipid A region of

Indexed as

choleracontinuous manufacturing (CM)Economic ModelingLMIC (low and middle income countries)mAb—monoclonal antibodyperfusion bioreactor system

Identifiers

PMID42807280
PMCPMC13616801

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.