# Neoantigen immune responses in healthy volunteers: insights from multiple integrated keyhole limpet hemocyanin challenge studies on repeated immunization and response covariates

## TL;DR

Researchers studied immune responses in healthy volunteers using a keyhole limpet hemocyanin (KLH) challenge to understand variability in immune reactions and optimize study design.

## Contribution

The study integrates multiple KLH trials to identify covariates affecting immune responses and optimize KLH challenge protocols for pharmacodynamic evaluations.

## Key findings

- Three KLH immunizations significantly increased antibody levels and skin responses compared to fewer doses.
- A design with three immunizations and 24-hour skin imaging showed the highest statistical power.
- Age negatively correlated with systemic KLH responses but positively with local responses.

## Abstract

Investigational immunomodulatory drugs are often initially investigated in healthy volunteers, which lack drug-target engagement biomarkers, hampering evaluation of pharmacodynamic effects. A model such as the Keyhole Limpet Hemocyanin (KLH) neoantigen challenge induces a well-controlled adaptive immune response and can be used to study pharmacodynamic effects in healthy volunteers. To increase our understanding of sources of variability in KLH-induced responses, we integrated KLH data from multiple studies executed at our research institute and investigated the contribution of covariates to KLH challenge responses.

We performed a pooled analysis of seven KLH trials with standardized methodology and design. Included trials immunized participants with KLH one, two or three times, with an interval of 2 weeks, followed by subsequent intradermal KLH administration 2–3 weeks after the final immunization. Differences and correlations were calculated between anti-KLH IgM and IgG and skin perfusion, flare, and erythema. A mixed effects model analysis was performed to estimate variances and determine the effect of the number of immunizations and the systemic and local biomarkers on the sample size. Finally, the effect of covariates age, sex, and body mass index was analyzed.

A total of 68 participants were included: 42 participants were immunized with KLH once, 5 participants twice, and 21 participants three times. Three times immunization resulted in significantly higher antibody levels, cutaneous perfusion, and flare. A study design incorporating three immunizations and skin imaging at 24 h was found to have the most robust statistical power. Lastly, the systemic KLH response correlated negatively with age and positively with local KLH responses.

This analysis provides a basis for the design of future clinical studies with KLH challenges. These data provide further insights into the performance of the human KLH challenge, which will facilitate the implementation of this immune challenge model in future clinical pharmacology studies.