Guillain-Barré syndrome with T-cell receptor gene clonal rearrangement following COVID-19 vaccination: a case report
The occurrence of Guillain-Barré syndrome (GBS) following coronavirus disease 2019 (COVID-19) vaccination have been documented; however, its pathogenesis remains unclear. We present a case of GBS associated with T-cell receptor (TCR) clonal rearrangement after COVID-19 vaccination. A previously healthy 60-year-old man developed fever, skin rash, general fatigue, and generalized urticaria after receiving his third vaccine dose (Spikevax, Moderna). No adverse events occurred after his first and second doses (COMIRNATY, Pfizer). Within 4 weeks of vaccination, the patient experienced progressive limb weakness and gait instability, and was referred to our hospital. Nerve conduction studies revealed increased distal latency, reduced compound muscle action potential amplitudes, decreased motor nerve conduction velocities, and diminished sensory nerve action potentials. Positron emission tomography-computed tomography showed systemic lymphadenopathy, splenomegaly, and increased splenic and bone marrow uptake. Bone marrow biopsy and peripheral blood analysis demonstrated TCR clonal rearrangement, which resolved by day 115 post-vaccination. Based on clinical progression, electrophysiological findings, and worsening neurological symptoms, a diagnosis of GBS was made. This case suggests that aberrant T-cell clonal expansion may contribute to GBS development following COVID-19 vaccination. To our knowledge, this is the first report describing TCR gene clonal rearrangement following COVID-19 vaccination.
- # Coronavirus Disease 2019 Vaccination
- # Decreased Motor Nerve Conduction Velocities
- # T-cell Receptor Clonal Rearrangement
- # Compound Muscle Action Potential Amplitudes
- # Guillain-Barré Syndrome
- # Clonal Rearrangement
- # Diagnosis Of Guillain-Barré Syndrome
- # Bone Marrow Uptake
- # Gene Clonal Rearrangement
- # T-cell Receptor
21
- 10.1186/s12883-014-0202-3
- Oct 15, 2014
- BMC Neurology
30
- 10.1684/ecn.2019.0424
- Mar 1, 2019
- European Cytokine Network
815
- 10.1212/wnl.51.4.1110
- Oct 1, 1998
- Neurology
3
- 10.1007/s00134-024-07345-3
- Mar 1, 2024
- Intensive Care Medicine
171
- 10.1002/ana.26143
- Jun 22, 2021
- Annals of Neurology
69
- 10.1016/j.clineuro.2021.106887
- Aug 13, 2021
- Clinical Neurology and Neurosurgery
9
- 10.3389/fneur.2024.1396642
- Jun 5, 2024
- Frontiers in neurology
21
- 10.3389/fimmu.2023.1078197
- Feb 15, 2023
- Frontiers in Immunology
24
- 10.1016/j.cellimm.2020.104273
- Jan 5, 2021
- Cellular Immunology
36
- 10.1007/s12185-023-03660-5
- Sep 20, 2023
- International Journal of Hematology
- Research Article
1
- 10.1016/j.amj.2022.02.007
- Mar 17, 2022
- Air Medical Journal
Vaccination
- Front Matter
4
- 10.1016/j.fertnstert.2021.05.083
- May 14, 2021
- Fertility and Sterility
Should women undergoing in vitro fertilization treatment or who are in the first trimester of pregnancy be vaccinated immediately against COVID-19
- Research Article
- 10.1016/j.ptdy.2021.07.022
- Aug 1, 2021
- Pharmacy Today
Immunization Update 2021
- Supplementary Content
21
- 10.1007/s10238-022-00836-x
- May 24, 2022
- Clinical and Experimental Medicine
Hyperviscosity syndrome (HVS) recently emerged as a complication of coronavirus disease 2019 (COVID-19) and COVID-19 vaccines. Therefore, the objectives of this critical review are to establish the association between COVID-19 and COVID-19 vaccines with the development of HVS. HVS may develop in various viral infections due to impairment of humoral and cellular immunity with elevation of immunoglobulins. COVID-19 can increase blood viscosity (BV) through modulation of fibrinogen, albumin, lipoproteins, and red blood cell (RBC) indices. HVS can cause cardiovascular and neurological complications in COVID-19 like myocardial infarction (MI) and stroke. HVS with or without abnormal RBCs function in COVID-19 participates in the reduction of tissue oxygenation with the development of cardio-metabolic complications and long COVID-19. Besides, HVS may develop in vaccine recipients with previous COVID-19 due to higher underlying Ig concentrations and rarely without previous COVID-19. Similarly, patients with metabolic syndrome are at the highest risk for propagation of HVS after COVID-19 vaccination. In conclusion, COVID-19 and related vaccines are linked with the development of HVS, mainly in patients with previous COVID-19 and underlying metabolic derangements. The possible mechanism of HVS in COVID-19 and related vaccines is increasing levels of fibrinogen and immunoglobulins. However, dehydration, oxidative stress, and inflammatory reactions are regarded as additional contributing factors in the pathogenesis of HVS in COVID-19. However, this critical review cannot determine the final causal relationship between COVID-19 and related vaccines and the development of HVS. Prospective and retrospective studies are warranted in this field.
- Research Article
- 10.1097/jom.0000000000002770
- Dec 14, 2022
- Journal of Occupational & Environmental Medicine
Ethical Considerations Surrounding Employment Mandated Coronavirus Disease 2019 Vaccination and Allergy Skin Testing for the Coronavirus Disease 2019 Vaccine.
- Research Article
1
- 10.1542/hpeds.2023-007660
- Aug 5, 2024
- Hospital pediatrics
Data on US caregiver perceptions on coronavirus disease 2019 (COVID-19) and COVID-19 vaccination are limited. We identified trends in and associations with COVID-19 vaccine hesitancy in caregivers of hospitalized children. Cross-sectional surveys on pediatric COVID-19 disease and vaccine attitudes, behaviors, and beliefs were administered across study years (December 8, 2020-April 5, 2021, November 30, 2021-March 15, 2022, and October 26, 2022-March 15, 2023). English and Spanish-speaking caregivers of hospitalized children ages 6 months to 11 years were included. General vaccine hesitancy was assessed using the Parent Attitudes about Childhood Vaccines survey. Of 1268 caregivers from diverse backgrounds, one-third vaccinated or intended to vaccinate their child. Half endorsed fear of their child receiving the COVID-19 vaccine and were concerned the vaccine was new. Over time, more believed "the COVID-19 vaccine does not work" and fewer agreed "children who are otherwise healthy can die from COVID-19." Study season (2022-2023), older child age, higher income, child receipt of influenza vaccine, caregiver receipt of COVID-19 vaccine, and not being worried about vaccine novelty were positively associated with child vaccination. Intent to vaccinate was negatively associated with study season (2022-2023), Parent Attitudes about Childhood Vaccines score ≥50, lack of child influenza and caregiver COVID-19 vaccination, lack of fear of their child "getting COVID-19" and being "worried that the COVID-19 vaccine is new." The majority who intended to vaccinate were willing to immunize before discharge. Vaccine novelty and perceived lack of need were associated with refusal. Caregiver COVID-19 and child influenza vaccine acceptance were positively associated with COVID-19 vaccine acceptance. The inpatient setting offers the opportunity to improve vaccine uptake.
- Research Article
3
- 10.1002/joa3.12721
- Apr 21, 2022
- Journal of arrhythmia
Frequency of vaccine-associated syncope after COVID-19 vaccination in adolescents.
- Research Article
23
- 10.1016/j.molmed.2022.04.012
- May 3, 2022
- Trends in molecular medicine
COVID-19 vaccines in pregnancy.
- Research Article
3
- 10.1016/j.jgo.2022.07.005
- Jul 15, 2022
- Journal of Geriatric Oncology
Updated International Society of Geriatric Oncology COVID-19 working group recommendations on COVID-19 vaccination among older adults with cancer
- Discussion
251
- 10.1016/s0140-6736(20)30763-7
- Mar 31, 2020
- Lancet (London, England)
Ensuring global access to COVID-19 vaccines
- Research Article
17
- 10.1212/wnl.0000000000207900
- Oct 18, 2023
- Neurology
Existing data regarding occurrence of Guillain-Barré syndrome (GBS) after coronavirus disease 2019 (COVID-19) infection and vaccination are inconclusive. We aimed to assess the association between GBS and both severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and COVID-19 vaccine. We conducted a nested case-control study in a cohort of 3,193,951 patients aged 16 years or older, without a diagnosis of prior GBS, from the largest health care provider in Israel. Participants were followed from January 1, 2021, until June 30, 2022, for the occurrence of GBS. Ten randomly selected controls were matched to each case of GBS on age and sex. We assessed both SARS-CoV-2 infection and COVID-19 vaccine administration in the prior 6 weeks in cases and controls. Overall, 76 patients were diagnosed with GBS during follow-up and were matched to 760 controls. A positive test for SARS-CoV-2 was detected in 9 (11.8%) cases and 18 (2.4%) controls. An administration of COVID-19 vaccine was detected in 8 (10.5%) cases (all Pfizer-BioNTech [BNT162b2] vaccine) and 136 (17.9%) controls (134 Pfizer-BioNTech vaccine). Multivariable conditional logistic regression models showed that the odds ratio for GBS associated with SARS-CoV-2 infection and COVID-19 vaccine administration was 6.30 (95% CI 2.55-15.56) and 0.41 (95% CI 0.17-0.96), respectively. The results were similar when exposure to SARS-CoV-2 infection or COVID-19 vaccine administration was ascertained in the prior 4 and 8 weeks, although did not reach statistical significance for COVID-19 vaccine at 4 weeks. Our study suggests that SARS-CoV-2 infection is associated with increased risk of GBS, whereas Pfizer-BioNTech COVID-19 vaccine is associated with decreased risk of GBS.
- Research Article
4
- 10.1542/peds.2021-050160
- May 1, 2021
- Pediatrics
* Abbreviations: CDC — : Centers for Disease Control and Prevention CMC — : children with medical complexity COVID-19 — : coronavirus disease 2019 The coronavirus disease 2019 (COVID-19) pandemic has created a national and global crisis. The United States has invested tremendous effort and resources to fast track severe acute respiratory syndrome coronavirus 2 vaccines from conception to market in 1 year, an amazing scientific achievement. Public health experts are now leading the distribution of COVID-19 vaccines. The Centers for Disease Control and Prevention (CDC) recommends that health care personnel be offered COVID-19 vaccination during the early phases of distribution. Health care personnel are broadly defined and include emergency medical service personnel, nurses and nursing assistants, physicians, technicians, therapists, dentists, dental hygienists and assistants, phlebotomists, pharmacists, students and trainees, contractual staff, dietary and food services staff, environmental services staff, and administrative staff. We strongly recommend that parents and family caregivers (collectively referred to as parents in this article) of children with medical complexity (CMC) be included in the early phases of vaccine distribution because they serve as essential frontline health care personnel. CMC have significant chronic health conditions that involve multiple organ systems, substantial health service needs, major functional limitations, and high health resource use. They have high levels of medical fragility, technology dependencies (tracheostomies, ventilators, feeding tubes, intrathecal baclofen infusion systems, and others), and psychosocial complexities. We identify CMC as those who have ≥3 organ systems affected (≥3 Feudtner … Address correspondence to Nancy A. Murphy, MD, FAAP, FAAPMR, Division of Pediatric Physical Medicine & Rehabilitation, Department of Pediatrics, School of Medicine, University of Utah, 81 North Mario Capecchi Dr, Salt Lake City, UT 84113. E-mail: nancy.murphy{at}hsc.utah.edu
- Research Article
83
- 10.4103/0972-2327.83087
- Jan 1, 2011
- Annals of Indian Academy of Neurology
Guillain–Barre syndrome (GBS) is an acute onset, usually monophasic immune-mediated disorder of the peripheral nervous system. The term GBS is often considered to be synonymous with acute inflammatory demyelinating polyradiculoneuropathy (AIDP), but with the increasing recognition of variants over the past few decades, the number of diseases that fall under the rubric GBS have grown to include axonal variants and more restricted variants, such as Miller Fisher syndrome (MFS) [Table 1].[1] Table 1 Guillain–Barre syndrome—clinical variants Epidemiology The reported incidence rates for GBS are 1–2 per 100,000 population.[2–4] The lifetime likelihood of any individual acquiring GBS is 1:1000.[5] The subtypes of GBS have different incidence rates in different parts of the world. In Europe and North America AIDP is dominant contributing to 90% of the cases. In contrast in China and Japan AMAN being the most common subtype.[6,7] The picture is intermediate when we look at other population. In Indian series the incidence of AIDP and AMAN are virtually equal although AMAN is more common in younger patients.[8] There seems to be a slight preponderance of AIDP in studies by Gupta et al[9] and by Meena et al (unpublished data from NIMS, Hyderabad). Available Indian literature indicates a peak incidence between June–July and Sept–October.[10] In western countries, GBS is common in the 5th decade,[11] but in India it occurs more commonly at a younger age.[10,12] GBS is equally common in men and women and can occur at any age. There is a male preponderance among the hospitalized population.[10,12]
- Research Article
71
- 10.1016/j.japh.2021.05.009
- May 21, 2021
- Journal of the American Pharmacists Association
COVID-19 and influenza vaccine hesitancy among college students
- Research Article
45
- 10.1111/ajt.16517
- Feb 28, 2021
- American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
Allergic reactions including anaphylaxis after receipt of the first dose of Moderna COVID-19 vaccine - United States, December 21, 2020-January 10, 2021.
- Supplementary Content
- 10.7774/cevr.2025.14.e32
- Jul 1, 2025
- Clinical and Experimental Vaccine Research
- Research Article
- 10.7774/cevr.2025.14.e29
- Jun 19, 2025
- Clinical and Experimental Vaccine Research
- Research Article
- 10.7774/cevr.2025.14.e28
- Jun 17, 2025
- Clinical and Experimental Vaccine Research
- Research Article
- 10.7774/cevr.2025.14.e26
- Jun 13, 2025
- Clinical and Experimental Vaccine Research
- Supplementary Content
- 10.7774/cevr.2025.14.e27
- Jun 13, 2025
- Clinical and Experimental Vaccine Research
- Research Article
- 10.7774/cevr.2025.14.e25
- May 22, 2025
- Clinical and Experimental Vaccine Research
- Research Article
- 10.7774/cevr.2025.14.e24
- May 21, 2025
- Clinical and Experimental Vaccine Research
- Research Article
- 10.7774/cevr.2025.14.e23
- Apr 15, 2025
- Clinical and Experimental Vaccine Research
- Research Article
- 10.7774/cevr.2025.14.e22
- Apr 14, 2025
- Clinical and Experimental Vaccine Research
- Research Article
- 10.7774/cevr.2025.14.e21
- Mar 31, 2025
- Clinical and Experimental Vaccine Research
- Ask R Discovery
- Chat PDF
AI summaries and top papers from 250M+ research sources.