Article Text

High antibody response to two-dose SARS-CoV-2 messenger RNA vaccination in patients with rheumatic and musculoskeletal diseases
  1. Jake A Ruddy1,2,
  2. Caoilfhionn Marie Connolly2,
  3. Brian J Boyarsky1,
  4. William A Werbel3,
  5. Lisa Christopher-Stine2,
  6. Jacqueline Garonzik-Wang1,
  7. Dorry L Segev1,4,
  8. Julie J Paik2
  1. 1Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
  2. 2Division of Rheumatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
  3. 3Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
  4. 4Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA
  1. Correspondence to Dr Dorry L Segev, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA; dorry{at}

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SARS-CoV-2 mRNA vaccination elicited high immunogenicity in immunocompetent people in the original vaccine trials,1 2 though recent studies have shown blunted immunogenicity in patients with rheumatic and musculoskeletal diseases (RMDs) after a single dose and case reports of non-response after two doses.3 4 We previously detailed antibody response in patients with RMD following the first dose of SARS-CoV-2 mRNA vaccination and herein report response and factors associated with response to two-dose vaccination in a larger cohort.

As previously reported,3 patients aged ≥18 years old with RMD were recruited to participate in this prospective, observational cohort via social media outreach to national RMD organisations between 12 July 2020 and 16 March 2021. Demographics, diagnoses and therapeutic regimens were collected via participant report through the Research Electronic Data Capture tool. One month after dose 2 (D2), participants underwent SARS-CoV-2 antibody testing on the semiquantitative Roche Elecsys anti-SARS-CoV-2 S enzyme immunoassay, which measures total antibody (IgM and IgG) to the SARS-CoV-2 S receptor-binding domain (RBD) protein,5 the target of the mRNA vaccines. Results range from <0.4 to >250 U/mL with a positive response defined as >0.79 U/mL. Associations were evaluated using Fisher’s exact and Wilcoxon rank-sum tests. Participants provided informed consent.

We studied 404 participants who received two doses of the SARS-CoV-2 mRNA vaccine (online supplemental table 1). The median (IQR) age was 44 (36–57), 96% were female, 9% were non-white, 49% received the Pfizer/BioNTech vaccine and 51% received Moderna, 4% had a prevaccination history of COVID-19 diagnosis and no participant reported postvaccination COVID-19 diagnosis. Most common diagnoses included inflammatory arthritis (45%) and systemic lupus erythematosus (22%). The most frequently prescribed medications were hydroxychloroquine (42%) and glucocorticoids (29%), while 51% were on combination therapy. Participants completed anti-RBD testing at a median of 29 days after D2.

Anti-SARS-CoV-2 RBD antibodies were positive in 378/404 (94%) participants (95% CI 91% to 96%) (online supplemental table 1). Median anti-RBD titre was above the upper limit of the assay (>250 U/mL), while lower median titres were observed in participants on regimens including mycophenolate (8 U/mL) and rituximab (<0.4 U/mL) (figure 1, online supplemental table 2). Tumour necrosis factor inhibitor use was associated with a positive antibody response (100% positive, p<0.001), while regimens including mycophenolate (73% positive, p<0.001), rituximab (26% positive, p<0.001) or glucocorticoids (82% positive, p<0.001) and a diagnosis of myositis (79% positive, p=0.01) were associated with a negative response. Of note, 4/5 (80%) negative responders with myositis and 18/21 (86%) negative responders on glucocorticoids were on regimens including mycophenolate or rituximab; all eight on glucocorticoid monotherapy had an anti-RBD titre >250 U/mL.

Figure 1

Anti-SARS-CoV-2 RBD antibody titre overall (n=403*) and by medications associated with a negative antibody response: mycophenolate included in regimen (n=41), rituximab included in regimen (n=19), glucocorticoid included in regimen (n=116) and glucocorticoid monotherapy (n=8) in patients with RMD after two-dose SARS-CoV-2 mRNA vaccination. Results range from <0.4 to >250 U/mL with positive antibody defined as an anti-SARS-CoV-2 RBD antibody titre >0.79 U/mL by the manufacturer; blue data points indicate median titre. *One titre value was missing from the total N (404). RBD, receptor binding domain; RMD, rheumatic and musculoskeletal disease.

In this study of humoral response to two-dose SARS-CoV-2 mRNA vaccination in patients with RMD, the vast majority of participants developed anti-RBD antibodies. Among negative responders, most were on regimens containing mycophenolate or rituximab. Glucocorticoid use was also associated with a negative response, though all of these individuals were on concomitant lymphocyte-depleting therapy. Compared with patients with RMD following D1 (74% seroconversion),3 this study showed increased seroconversion following two-dose vaccination (94% seroconversion). Similarly, seroconversion for those on mycophenolate-based regimens was 73% after two doses compared with 27% after D1, while the response for those on rituximab remained poor (33% seroconversion after D1, 26% seroconversion after D2). Despite a blunted humoral response in participants on these regimens, the rate of seroconversion was comparable with those seen in the original vaccine trials and existing studies on patients with RMD.1 2 6

Limitations of this study include a younger, generally female, racially homogenous population and limited information on immunomodulatory timing and dosage. Additionally, we did not evaluate for asymptomatic COVID-19 infection, and disease activity was not assessed.

While certain lymphocyte-depleting therapies were associated with failure to develop a humoral response, reassuringly, the majority of patients with RMD on a variety of immunosuppressive regimens had a robust antibody response to SARS-CoV-2 mRNA vaccination.

Ethics statements

Ethics approval

This study was approved by the Johns Hopkins School of Medicine Institutional Review Board (IRB00248540).


We also acknowledge the following individuals for their assistance with this study: Allan B Massie, PhD, Robin K Avery MD, Michael T Ou, BS, Ross S Greenberg, BS, and Iulia Barber, BS.


Supplementary materials

  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.


  • DLS and JJP are joint senior authors.

  • Handling editor Josef S Smolen

  • Twitter @CaoilfhionnMD

  • JAR and CMC contributed equally.

  • Contributors All authors contributed to study design. JAR and BJB contributed to data collection. All authors contributed to data analysis and interpretation. All authors contributed to drafting of the manuscript.

  • Funding This research was made possible with generous support of the Ben-Dov family. This work was supported by grant number F32DK124941 (Boyarsky), and K23DK115908 (Garonzik‐Wang) from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), K24AI144954 (Segev) from National Institute of Allergy and Infectious Diseases (NIAID), K23AR073927 (Paik) from National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAIM).

  • Disclaimer The analyses described here are the responsibility of the authors alone and do not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products or organisations imply endorsement by the US Government.

  • Competing interests DLS has the following financial disclosures: consulting and speaking honoraria from Sanofi, Novartis, CSL Behring, Jazz Pharmaceuticals, Veloxis, Mallincrodt and Thermo Fisher Scientific. LC-S has the following financial disclosures: consultant fees from Janssen, Boehringer-Ingelheim, Mallinckrodt, EMD-Serono, Allogene and ArgenX.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

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