PMID- 35815930 OWN - NLM STAT- MEDLINE DCOM- 20220712 LR - 20220830 IS - 1555-3892 (Electronic) IS - 0963-6897 (Print) IS - 0963-6897 (Linking) VI - 31 DP - 2022 Jan-Dec TI - Human Umbilical Cord Mesenchymal Stem Cells for Severe Neurological Sequelae due to Anti-N-Methyl-d-Aspartate Receptor Encephalitis: First Case Report. PG - 9636897221110876 LID - 10.1177/09636897221110876 [doi] LID - 09636897221110876 AB - Anti-N-methyl-d-aspartate (NMDA) receptor encephalitis is caused by altered patient immune reactions. This study reports the first patient with severe neurologic sequelae after NMDA receptor encephalitis treated with allogeneic umbilical cord-derived mesenchymal stem/stromal cells (UC-MSCs). A 5-year-old girl was diagnosed with NMDA receptor encephalitis and treated with immunosuppressive medicaments and intravenous immunoglobulin (IVIG). Despite intensive therapy, the patient's condition worsened so that allogenic UC-MSC therapy was contemplated. The patient received three intrathecal infusions of xeno- and serum-free cultured UC-MSCs at a dose of 10(6) cells/kg. At baseline and after each UC-MSC administration, the patient was examined by the German Coma Recovery Scale (CRS), the Gross Motor Function Classification System (GMFCS), the Gross Motor Function Measure-88 (GMFM-88), the Manual Ability Classification System (MACS), the Modified Ashworth Scale, and the Denver II test. Before cell therapy, she was in a permanent vegetative state with diffuse cerebral atrophy. Her cognition and motor functions improved progressively after three UC-MSC infusions. At the last visit, she was capable of walking, writing, and counting numbers. Control of urinary and bowel functions was completely recovered. Cerebral atrophy was reduced on brain magnetic resonance imaging (MRI). Overall, the outcomes of this patient suggest a potential cell therapy for autoimmune encephalitis and its neurological consequences. FAU - Nguyen Thanh, Liem AU - Nguyen Thanh L AUID- ORCID: 0000-0001-5444-1782 AD - Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Health Care System, Hanoi, Vietnam. AD - College of Health Science, VinUniversity, Hanoi, Vietnam. FAU - Hoang, Van T AU - Hoang VT AD - Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Health Care System, Hanoi, Vietnam. FAU - Le Thu, Huong AU - Le Thu H AD - Vinmec International Hospital, Hanoi, Vietnam. FAU - Nguyen, Phuong Anh Thi AU - Nguyen PAT AD - Vinmec International Hospital, Hanoi, Vietnam. FAU - Hoang, Duc M AU - Hoang DM AD - Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Health Care System, Hanoi, Vietnam. FAU - Ngo, Doan Van AU - Ngo DV AD - Vinmec International Hospital, Hanoi, Vietnam. FAU - Cao Vu, Hung AU - Cao Vu H AD - Vietnam National Children's Hospital, Hanoi, Vietnam. FAU - Nguyen Thi Bich, Van AU - Nguyen Thi Bich V AD - Vietnam National Children's Hospital, Hanoi, Vietnam. FAU - Heke, Michael AU - Heke M AD - Department of Biology, Stanford University, Stanford, CA, USA. LA - eng PT - Case Reports PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Cell Transplant JT - Cell transplantation JID - 9208854 RN - 0 (Receptors, N-Methyl-D-Aspartate) SB - IM MH - *Anti-N-Methyl-D-Aspartate Receptor Encephalitis/complications/diagnosis/therapy MH - Atrophy/complications MH - Child, Preschool MH - Disease Progression MH - Female MH - Humans MH - *Mesenchymal Stem Cells MH - Receptors, N-Methyl-D-Aspartate/therapeutic use MH - Umbilical Cord PMC - PMC9277426 OTO - NOTNLM OT - anti-NMDA receptor encephalitis OT - autoimmune encephalitis OT - mesenchymal stem cells OT - mesenchymal stromal cells OT - neurological sequelae COIS- Declaration of Conflicting Interests: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: L.N.T., V.T.H., H.L.T., P.A.T.N., D.M.H., and D.V.N. are employed by the not-for-profit Vinmec Healthcare System. M.H. declared an advisory role for Regenerative Medicine at Vinmec Healthcare System. EDAT- 2022/07/12 06:00 MHDA- 2022/07/14 06:00 PMCR- 2022/07/11 CRDT- 2022/07/11 08:43 PHST- 2022/07/11 08:43 [entrez] PHST- 2022/07/12 06:00 [pubmed] PHST- 2022/07/14 06:00 [medline] PHST- 2022/07/11 00:00 [pmc-release] AID - 10.1177_09636897221110876 [pii] AID - 10.1177/09636897221110876 [doi] PST - ppublish SO - Cell Transplant. 2022 Jan-Dec;31:9636897221110876. doi: 10.1177/09636897221110876.