Next-generation antibacterial vaccines & therapies

Precision antibacterial vaccines for the world's toughest infections

RhogenShield develops self-adjuvanting therapies built on outer membrane vesicles (OMVs) — targeting the bacteria behind colorectal cancer, tuberculosis, drug-resistant ESKAPE infections, and chronic diabetic foot ulcers.

OMV platform CRC · TB · ESKAPE · DFU Self-adjuvanting
Antibodies binding a target protein — precision molecular targeting
Our focus: OMV-based antibacterial vaccines & therapies Colorectal cancer Tuberculosis ESKAPE / AMR Diabetic foot ulcers
Our lead program in motion

OMVs engineered to carry colorectal-cancer epitopes

Outer membrane vesicles loaded with CRC-specific neoantigens and epitopes — the vaccine cargo at the heart of our colorectal cancer program.

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What drives us

Bacteria drive some of medicine's hardest problems — from the microbes implicated in colorectal cancer, to tuberculosis, to the drug-resistant ESKAPE pathogens behind chronic, non-healing wounds like diabetic foot ulcers. We're building self-adjuvanting, OMV-based vaccines and therapies to prevent and treat them.

The platform

OMV-based antibacterial platform

Outer membrane vesicles (OMVs) are nanoscale particles naturally shed by bacteria. They present bacterial antigens alongside built-in immune-activating signals — a proven, self-adjuvanting route to vaccines and therapies against bacterial disease.

Inside an OMV

The anatomy of an outer membrane vesicle

A cutaway of an OMV — an LPS-rich outer membrane studded with lipoproteins, enclosing periplasm-derived cargo such as enzymes, toxins and nucleic acids. This natural payload is exactly what our vaccines and therapies are engineered to harness.

How OMV vaccines work
1 Bacteria shed OMVs 2 OMVs display antigens 3 Antibody & immune response

Self-adjuvanting

OMVs carry natural immune-activating signals — strong responses without a separate adjuvant.

Modular & fast

Reprogram against a new pathogen by swapping the antigens the OMVs display.

Broad immunity

Engages antibody and T-cell responses — valuable against intracellular and resistant bacteria.

Scalable & affordable

Grown by microbial fermentation — a route to high volumes at low cost for wider access.

Our programs

The diseases we target

We apply our OMV platform across four high-burden bacterial challenges where better prevention and treatment are urgently needed.

Oncobacterial

Colorectal cancer

An oncomicrobial vaccine targeting tumour-associated bacteria implicated in colorectal cancer (CRC).

Mycobacterium

Tuberculosis (Mtb)

An antibacterial vaccine against Mycobacterium tuberculosis, one of the world's deadliest infections.

Drug-resistant

ESKAPE pathogens

Vaccines against the ESKAPE panel of antibiotic-resistant bacteria driving antimicrobial resistance (AMR).

Chronic wound infection

Diabetic foot ulcers

An engineered OMV therapy, delivered in a gel matrix, to fight the resistant infections that keep diabetic foot ulcers (DFU) from healing.

Colorectal cancer

An oncomicrobial vaccine for colorectal cancer

Specific tumour-associated bacteria are enriched in colorectal tumours, where they promote inflammation and cancer progression.

Our OMV-based oncomicrobial vaccine presents these bacteria-derived antigens to the immune system — activating T-cells that migrate to the tumour and attack the microbial environment that supports the cancer.

Engineered OMV gel matrix and oleogel-based film applied to a diabetic foot ulcer
Diabetic foot ulcers

An engineered OMV gel matrix for diabetic foot ulcers

Diabetic foot ulcers are chronic, hard-to-heal wounds fuelled by drug-resistant bacteria and biofilms — a leading cause of amputation.

We're developing engineered OMVs delivered in an oleogel-based film — a gel matrix applied directly to the wound to target the underlying infection and support healing.

Careers

Join our mission

We're a small, ambitious team building vaccines against the world's toughest bacteria. If that excites you, we'd love to hear from you.

Now hiring

Scientist / Postdoctoral Fellow — Tuberculosis (TB) Vaccine Development

Full-time On-site · C-CAMP, Bengaluru R&D · Vaccine science

Lead the development of our tuberculosis (TB) vaccine — from antigen design through preclinical immunology and characterisation.

What we're looking for

  • A PhD in immunology, microbiology, vaccinology or a related field — or equivalent postdoctoral research experience.
  • Hands-on experience in molecular biology, bacterial culture, and/or immunoassays; experience in tuberculosis or vaccine development is a plus.
  • A collaborative, self-driven approach and a passion for translating vaccine science into real-world impact.
Apply — email us Send your CV and a short cover note to Director at rhogenshield.com
Get in touch

Partner with us

Whether you're an investor, researcher, manufacturer or public-health partner, we'd love to hear from you.

LocationRhogenShield Vaccines Pvt. Ltd.
C-CAMP (Centre for Cellular and Molecular Platforms)
GKVK Post, Bellary Road, Bengaluru 560065
Karnataka, India

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