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Published on: February 5, 2020
Immunological Monitoring During Anti-CD20 Therapies to Predict Infection Risk and Treatment Response in Multiple
Gabriel Torres Iglesias1, Ana Martínez-Feito2, Laura Otero-Ortega1
1Neurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neurology and Cerebrovascular Disease Group, Neuroscience Area of Hospital La Paz Institute for Health Research IdiPAZ, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.
Immunological monitoring of multiple sclerosis (MS) patients on anti-CD20 therapy can predict infections. Baseline immune cell levels and immunoglobulin G (IgG) hypogammaglobulinemia are key risk factors for infection and treatment response.
Area of Science:
- Neuroimmunology
- Immunology
- Infectious Diseases
Background:
- Disease-modifying therapies (DMTs) for multiple sclerosis (MS) require immunological monitoring to anticipate infectious complications.
- Anti-CD20 treatments are widely used for MS, but their impact on patient immunodeficiency requires further investigation.
- Identifying predictive immunological markers for infection risk and treatment response is crucial for managing MS patients.
Purpose of the Study:
- To determine if anti-CD20 therapies in MS patients induce immunodeficiency.
- To evaluate specific immunological parameters for predicting infection risk.
- To assess the potential of immunological markers in predicting treatment response in MS patients.
Main Methods:
- Retrospective, observational, single-centre study of MS patients treated with ocrelizumab or rituximab (2017-2023).
- Analysis of lymphocyte subpopulations (T, B, NK) and immunoglobulin levels (IgG, IgA, IgM) at baseline and 24-month follow-up.
- Detailed baseline B cell analysis, including CD20 depletion assessment during follow-up.
Main Results:
- Sixty-four percent of patients experienced infections, primarily COVID-19; IgG hypogammaglobulinemia was a significant risk factor.
- Infections correlated with reduced mature memory B cells and lower NK cell percentages.
- Lower naïve and mature memory B cell proportions were linked to inflammatory activity and disease progression, respectively; lack of CD20 depletion predicted clinical worsening.
Conclusions:
- Baseline immunophenotyping and ongoing immunological monitoring are valuable for predicting infection risk in MS patients.
- These assessments can also help predict the efficacy of anti-CD20 therapies in multiple sclerosis.
- Immunological monitoring aids in personalized treatment strategies for MS patients receiving anti-CD20 agents.
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