Completed Infection & Immunity Digestion, Kidneys & Other Organs

Development of an invasive non-typhoidal Salmonella human challenge model

In plain English

AI plain-English summary

A handful of volunteers will swallow a carefully measured dose of live Salmonella bacteria to test whether a controlled human infection model can speed up vaccine development for a deadly form of the disease. Invasive non-typhoidal Salmonella (iNTS) kills roughly one in five people it infects, mostly children and HIV-positive adults in sub-Saharan Africa. Several candidate vaccines exist, but testing them in the field requires huge, expensive phase-3 trials because the disease is relatively rare even in affected regions. Controlled human infection models (CHIMs) have already accelerated vaccines for cholera and typhoid fever. This project aims to build a similar model for iNTS, allowing researchers to generate preliminary efficacy data from small groups of volunteers rather than thousands of people in the field. If the model works, it could dramatically cut the cost and time needed to bring an iNTS vaccine to licensure. The approach would also let researchers study immune responses, bacterial shedding, and transmission in ways that are nearly impossible to capture in traditional field trials. This is applied research with a clear practical endpoint: a faster route to a vaccine that could save tens of thousands of lives each year.

View original technical description
Our vision is to develop an iNTS CHIM programme that dovetails with future iNTS-vaccine efficacy studies, whilst simultaneously addressing fundamental questions on the immunological basis of susceptibility to iNTS disease. Several iNTS candidate vaccines are in development, but the epidemiology of iNTS disease is such that phase-3 trials require a large financial and time commitment before an efficacy readout is obtained. There are several instances where CHIM studies have accelerated vaccine candidates through to licensure, in particular for enteric pathogens such as Vibrio cholerae and Salmonella Typhi. We contend that a safe, reproducible, and well-designed CHIM – with clinically meaningful endpoints – will allow the field to build upon insights from animal models and could have an important role in accelerating vaccine development for iNTS. We will work closely with vaccine developers and regulators to identify a pathway for iNTS vaccine assessment in a CHIM. In particular, we envisage that phase-2 studies could include a CHIM to generate preliminary efficacy-indicating estimates and yield data that would otherwise be difficult to capture in phase 3 efficacy studies (e.g. stool shedding, transmission studies, longitudinal immune response to vaccination and challenge).

View the original record at the funder ↗

Researchers

Andrew Pollard (EPMC Awardee)Christopher Chiu (EPMC Awardee)Graham Cooke (EPMC Awardee)Jay Hinton (EPMC Awardee)Jessica White (EPMC Awardee)Malick Gibani (EPMC Awardee)Melita Gordon (EPMC Awardee)Rahsan Erdem (EPMC Awardee)Robert Choy (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

CHANTS: The Development of a non-typhoidal Salmonella human challenge model: A safety and dose escalation study.
The Development of a non-typhoidal Salmonella human challenge model: A safety and dose escalation study.
Advancing a GMMA-based vaccine against invasive non-typhoidal salmonellosis through Phase 1 trial in Europe and sub-Saharan Africa
Innovative experimental approaches to determine how the human microbiota prevents Salmonella Typhimurium infections
Manufacture of a GMP SARS-CoV-2 challenge agent

Original classification

Innovations AIGH Enterics Flagship

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.