Evidence map›Paper›PMID 37675826›Full record

ArticleAnnals of clinical and translational neurology2023

Anti-CD20 monoclonal antibody therapy in postpartum women with neurological conditions.

Annika Anderson, William Rowles, Shane Poole, Ayushi Balan, Carolyn Bevan, Rachel Brandstadter, Andrea I Ciplea, Joanna Cooper, Michelle Fabian, Thomas W Hale and 13 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06940323 (Pregnancy Registry, Infants, Serum/Milk Analysis), which is not on this map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06940323 recruitingnot on this map

Pregnancy Registry, Infants, Serum/Milk Analysis (PRISMA): Pregnancy Registry for Women With Chronic Conditions

TypeobservationalSponsorUniversity of California, San FranciscoRan2017 to 2035Enrolled250ConditionsMultiple Sclerosis, Clinically Isolated Syndrome, NMOSD, Myasthenia Gravis
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Maternal disease control and pregnancy outcomes with anti-CD20 therapy versus natalizumab in multiple sclerosis: a systematic review.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Safety of Drugs in Breastfeeding Women With CKD.Kidney international reports · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Topical review: Lactation and use of DMTs in women with MS.Multiple sclerosis (Houndmills, Basingstoke, England) · 2024
    Review
  13. Review
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 15 institutions in 4 countries.

Annika AndersonUCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.ORCID 0000-0002-7288-6344
William RowlesUCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.
Shane PooleUCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.
Ayushi BalanUCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.
Carolyn BevanDepartment of Neurology, Northwestern University, Chicago, Illinois, USA.
Rachel BrandstadterDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Andrea I CipleaDepartment of Neurology, Ruhr University Bochum, Bochum, Germany.
Joanna CooperSutter East Bay Medical Group, Lafayette, California, USA.
Michelle FabianIcahn School of Medicine at Mount Sinai, New York, New York, USA.
Thomas W HaleTexas Tech University Health Sciences Center, Amarillo, Texas, USA.
Dina JacobsDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Mihir KakaraDepartment of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Kristen M KryskoDivision of Neurology, Department of Medicine, St Michael's Hospital, University of Toronto, Toronto, ON, Canada.ORCID 0000-0003-0090-597X
Erin E LongbrakeDepartment of Neurology, Yale University, New Haven, Connecticut, USA.ORCID 0000-0002-1179-3937
Jacqueline MarcusDepartment of Neurology, Kaiser Permanente San Francisco, San Francisco, California, USA.
Pavle RepovicDepartment of Neurology, Swedish Medical Center, Seattle, Washington, USA.
Claire S RileyDepartment of Neurology, Columbia University Irving Medical Center, New York, New York, USA.
Andrew R RomeoDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.
Alice RutatangwaUCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.ORCID 0000-0003-0843-7947
Timothy WestRocky Mountain MS Center, Salt Lake City, Utah, USA.
Kerstin HellwigDepartment of Neurology, Ruhr University Bochum, Bochum, Germany.
Sara C LaHueUCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.
Riley BoveUCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.
University of California, San Francisco · USUniversity of Pennsylvania · USUniversity Hospitals of the Ruhr-University of Bochum · DEBuck Institute for Research on Aging · USColumbia University Irving Medical Center · USIcahn School of Medicine at Mount Sinai · USKaiser Permanente San Francisco Medical Center · USNorthwestern University · USRocky Mountain Multiple Sclerosis Clinic · USSt. Michael's Hospital · CASutter Medical Center · USSwedish Medical Center · USTexas Tech University · USUniversity of Michigan · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Training in Healthcare Financing, Organization and Delivery for Aging PopulationsT32AG051090 · NIA · UNIVERSITY OF PENNSYLVANIA · PI PAULY, MARK, WERNER, RACHEL M · 2015 to 2019
$652k
AHRQ HHS T32 HS026116NCATS NIH HHS UL1 TR001863NIA NIH HHS T32 AG051090
6 · The paper itself

Abstract

objectivePostpartum, patients with multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) have increased risk for disease activity. Anti-CD20 IgG1 monoclonal antibodies (mAb) are increasingly used as disease-modifying therapies (DMTs). Patients may wish to both breastfeed and resume DMT postpartum. This study aimed to determine the transfer of anti-CD20 IgG1 mAbs, ocrelizumab, and rituximab (OCR/RTX), into mature breastmilk and describe maternal and infant outcomes.

methodsFifty-seven cis-women receiving OCR/RTX after 59 pregnancies and their infants were enrolled and followed up to 12M postpartum or 90 days post-infusion. Breastmilk was collected pre-infusion and serially up to 90 days and assayed for mAb concentration. Medical records and patients' questionnaire responses were obtained to assess neurologic, breastfeeding, and infant development outcomes.

resultsThe median average concentration of mAb in breastmilk was low (OCR: 0.08 μg/mL, range 0.05-0.4; RTX: 0.03 μg/mL, range 0.005-0.3). Concentration peaked 1-7 days post-infusion in most (77%) and was nearly undetectable after 90 days. Median average relative infant dose was <1% (OCR: 0.1%, range 0.07-0.7; RTX: 0.04%, range 0.005-0.3). Forty-three participants continued to breastfeed post-infusion. At 8-12 months, the proportion of infants' growth between the 3rd and 97th World Health Organization percentiles did not differ for breastfed (36/40) and non-breastfed (14/16, p > 0.05) infants; neither did the proportion with normal development (breastfed: 37/41, non-breastfed: 11/13; p > 0.05). After postpartum infusion, two mothers experienced a clinical relapse.

interpretationThese confirm minimal transfer of mAb into breastmilk. Anti-CD20 mAb therapy stabilizes MS activity before conception to the postpartum period, and postpartum treatments appears to be safe and well-tolerated for both mother and infant.

Indexed as

Antineoplastic AgentsMultiple SclerosisAntibodies, MonoclonalChildFemaleHumansImmunoglobulin GInfantPostpartum PeriodPregnancyRituximabAntibodies, MonoclonalAntineoplastic AgentsImmunoglobulin GRituximab

Identifiers

PMID37675826
PMCPMC10647007
OpenAlexW4386502014

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.