Immune alterations in schizophrenia and the effects of a therapeutic antibody: a neuroimaging study - Scorecard - MDSpire

Immune alterations in schizophrenia and the effects of a therapeutic antibody: a neuroimaging study

  • By

  • Yuya Mizuno

  • Ines Carreira Figueiredo

  • Toby Pillinger

  • Guy Hindley

  • Luke Baxter

  • Sita Parmar

  • Maria C Lobo

  • Jacek G Donocik

  • Ivana Rosenzweig

  • Anish Gupta

  • Ilaria Callegari

  • Sami Jeljeli

  • Joel T Dunn

  • Alexander Hammers

  • Ramla Awais

  • Kerstin Sander

  • Erik Årstad

  • Marios Politis

  • Julia J Schubert

  • Mattia Veronese

  • Federico E Turkheimer

  • Tiago Reis Marques

  • Oliver D Howes

  • December 1, 2025

  • 0 min

Share

Clinical Scorecard: Neuroimaging Insights into Immune Changes in Schizophrenia and the Impact of a Therapeutic Antibody

At a Glance

CategoryDetail
ConditionSchizophrenia with first-episode psychosis
Key MechanismsElevated 18 kDa translocator protein (TSPO) expression indicating neuroinflammation, primarily involving microglia and astrocytes
Target PopulationPatients with first-episode psychosis symptomatic despite antipsychotic treatment
Care SettingSpecialized psychiatric and neuroimaging research centers

Key Highlights

  • Baseline TSPO levels in grey matter, especially temporal lobe, are elevated in first-episode psychosis patients compared to healthy controls.
  • Natalizumab, a monoclonal antibody, crosses the blood–brain barrier and is well tolerated in schizophrenia patients.
  • Natalizumab treatment modestly improves symptoms but does not significantly alter TSPO PET binding, suggesting TSPO elevation may reflect non-microglial cell expression.

Guideline-Based Recommendations

Diagnosis

  • Use 18F-DPA-714 PET imaging to quantify TSPO levels as a biomarker of neuroinflammation in first-episode psychosis.
  • Assess symptom severity with the Positive and Negative Syndrome Scale (PANSS).

Management

  • Consider natalizumab as an add-on treatment for patients with inadequate response to antipsychotics, noting modest symptom improvement.
  • Continue standard antipsychotic treatment alongside investigational immune-targeted therapies.

Monitoring & Follow-up

  • Perform baseline and follow-up TSPO PET imaging to evaluate neuroinflammation status.
  • Monitor clinical symptoms using PANSS at baseline and after treatment.
  • Observe for adverse events related to natalizumab, although serious events were not reported.

Risks

  • Natalizumab was well tolerated with no serious treatment-related adverse events in this study.
  • The functional relevance of TSPO changes remains unclear; lack of TSPO reduction despite symptom improvement suggests complexity in immune involvement.

Patient & Prescribing Data

First-episode psychosis patients with persistent symptoms despite antipsychotic treatment

Natalizumab crosses the blood–brain barrier and leads to modest symptom improvement without significant changes in TSPO PET binding.

Clinical Best Practices

  • Use TSPO PET imaging to identify neuroinflammatory status in schizophrenia research settings.
  • Incorporate immune-targeted therapies cautiously, recognizing current evidence shows modest clinical benefit.
  • Further research is needed to clarify TSPO cellular specificity and its role as a biomarker in psychosis.

References

Original Source(s)

Related Content