# Lack of molecular mimicry between HPV vaccine L1 antigen and human proteins by a computational analysis

**Authors:** Kazuhiro Nishioka, Kentaro Sekiyama, Reona Shiro, Ikuo Tsunoda, Noriomi Matsumura

PMC · DOI: 10.1007/s10147-026-02961-z · International Journal of Clinical Oncology · 2026-01-08

## TL;DR

This study shows that HPV vaccines do not cause autoimmune reactions due to molecular mimicry, as no identical protein sequences were found between HPV and human proteins.

## Contribution

The study refutes flawed claims about HPV vaccine safety by demonstrating the absence of exact molecular mimicry with human proteins.

## Key findings

- No human epitopes had identical amino acid sequences to HPV16L1 epitopes.
- HPV16L1 had fewer instances of partial molecular mimicry compared to HBV and RSV.
- The findings suggest HPV vaccines do not induce cross-reactive autoantibodies.

## Abstract

Although human papillomavirus (HPV) vaccines effectively prevent cervical cancer, the HPV vaccination rates in Japan remain low because of concerns about alleged neurological adverse events. Darja Kanduc proposed a flawed hypothesis that molecular mimicry between HPV and human proteins could induce cross-reactive antibodies, causing autoimmune organ damage, even when only the portions of amino acid (AA)-sequences of the epitopes were identical between HPV and human proteins.

In this study, we conducted the same computational data analysis as Kanduc, using 22 linear epitopes (9–23 AA-length) of the HPV type 16 L1 protein (HPV16L1) registered in the database.

We found that no human epitopes had identical AA-sequences to any HPV16L1 epitopes, demonstrating that HPV16L1 had no molecular mimicry with linear epitopes that have the potential to induce cross-reactive autoantibodies. On the other hand, we identified various numbers of human protein epitopes whose AA-sequences were partially identical with epitopes of HPV16L1, hepatitis B virus (HBV), and respiratory syncytial virus (RSV). We found that HPV16L1 had a smaller number of such proteins having “partial molecular mimicry” than HBV and RSV.

Our current in silico analysis provided no evidence that HPV vaccinations could induce cross-reactive autoantibodies. The flawed molecular mimicry data should not be used as a scientific basis for alleged HPV vaccine-induced adverse events.

The online version contains supplementary material available at 10.1007/s10147-026-02961-z.

## Linked entities

- **Diseases:** cervical cancer (MONDO:0002974)

## Full-text entities

- **Diseases:** cervical cancer (MESH:D002583), autoimmune organ damage (MESH:D001327), neurological adverse (MESH:D009461)
- **Species:** Homo sapiens (human, species) [taxon 9606], Hepatitis B virus (no rank) [taxon 10407], Human papillomavirus (species) [taxon 10566], Respiratory syncytial virus (no rank) [taxon 12814]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12932383