# The Presence of Heat Shock Protein 70 (HSP70) Antibodies in Bilateral Meniere’s Disease: A Case Report

**Authors:** Stephanie Nagy, Marc M Kesselman

PMC · DOI: 10.7759/cureus.87843 · Cureus · 2025-07-13

## TL;DR

This case report explores a rare instance of bilateral Meniere’s Disease in a patient with HSP70 antibodies, suggesting a possible autoimmune link.

## Contribution

The report adds to the limited literature on HSP70 antibodies in bilateral Meniere’s Disease and highlights potential autoimmune associations.

## Key findings

- A 29-year-old female presented with bilateral Meniere’s Disease and HSP70 antibodies.
- The case suggests an autoinflammatory mechanism may contribute to Meniere’s Disease pathology.
- Bilateral MD is rare and may be associated with autoimmune factors like HSP70 antibodies.

## Abstract

Meniere’s disease (MD) is a chronic, idiopathic inner ear disorder characterized by episodes of vertigo, fluctuating sensorineural hearing loss, tinnitus, aural fullness, gait disturbances, and postural instability. The pathophysiology is most commonly thought to be due to either an excess of endolymphatic fluid secretion or a failure to resorb the fluid into the subarachnoid space. The distension of the endolymphatic space disrupts the auditory and vestibular systems, leading to the symptoms experienced. Postulated causes of MD have been linked to allergies, genetic mutations, epigenetic factors, and alterations in anatomy, but an autoimmune cause is currently the strongest hypothesis. Specifically, the expansion of the endolymphatic space has been found to trigger the release of heat shock protein 70 (HSP70) antibodies, leading to MD. Although a causal link remains unconfirmed, these findings suggest an underlying autoinflammatory mechanism, warranting further investigation. We present a 29-year-old female who has bilateral MD, a rare finding in itself, in addition to being positive for HSP70 antibodies. This case underscores the importance of recognizing the potential autoimmune associations of MD, particularly in bilateral presentations, and contributes to the limited literature linking HSP70 antibodies to disease pathology and potential therapeutic targets.

## Linked entities

- **Proteins:** HSPA1A (heat shock protein family A (Hsp70) member 1A)

## Full-text entities

- **Genes:** HSPA4 (heat shock protein family A (Hsp70) member 4) [NCBI Gene 3308] {aka APG-2, HEL-S-5a, HS24/P52, HSPH2, RY, hsp70}
- **Diseases:** autoinflammatory (MESH:D056660), tinnitus (MESH:D014012), sensorineural hearing loss (MESH:D006319), allergies (MESH:D004342), MD (MESH:D008575), instability (MESH:D043171), inner ear disorder (MESH:D007759), gait disturbances (MESH:D020233), vertigo (MESH:D014717)

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12342110/full.md

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Source: https://tomesphere.com/paper/PMC12342110