How IL-6 and SHANK3 changes affect brain connections in autism

Interleukin-6 induced synaptic dysgenesis in wild type vs. Shank3 mice

NIH-funded research Rutgers Biomedical and Health Sciences · NIH-11300958

Researchers will briefly raise the immune protein IL-6 in young mice with a SHANK3 gene change to look for worsening of autism-like brain wiring and behaviors.

Quick facts

Grant typeR03 grant
Study typeNIH-funded research
Funding institutionRutgers Biomedical and Health Sciences NIH-funded
Lab location1 site (Newark, UNITED STATES)
Project IDNIH-11300958 on NIH RePORTER

What this research studies

This project uses mice that carry a SHANK3 gene alteration linked to Phelan-McDermid/22q13 deletion and gives short doses of the immune protein IL-6 shortly after birth. The team will compare mice with one SHANK3-altered copy to normal mice, treating them with either IL-6 or a harmless solution and then tracking social interaction, repetitive behaviors, communication, and learning as they mature. Researchers will also examine brain synapses and cells to see how early IL-6 exposure changes neural connections at the cellular level. The goal is to model how a brief immune event during early development might interact with genetic vulnerability to produce autism-related changes.

Who could benefit from this research

Good fit: People with SHANK3-related autism (Phelan-McDermid syndrome) or families affected by 22q13 deletion who are interested in research on gene–environment causes may find this work most relevant.

Not a fit: Patients without SHANK3 or 22q13-related autism and those seeking immediate clinical treatments are unlikely to directly benefit from this preclinical mouse research.

Why it matters

Potential benefit: If successful, this work could clarify how early immune events and SHANK3-related genetics combine to produce autism traits, guiding future prevention or targeted therapies.

How similar studies have performed: Previous animal work has linked maternal IL-6 or immune activation to autism-like outcomes, but combining IL-6 exposure with a SHANK3 genetic model is a new, less-tested approach.

Where this research is happening

Newark, UNITED STATES

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Conditions 22q13 deletion syndrome
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.