Therapeutic plasma exchange decreases plasma anti-SARS-CoV-2 spike IgG without increasing the proximate incidence of COVID-19.

COVID-19 SARS-CoV-2 anti-SARS-CoV-2 spike immunoglobulin anti-spike IgG anti-spike immunoglobulin apheresis therapeutic plasma exchange

Journal

Journal of clinical apheresis
ISSN: 1098-1101
Titre abrégé: J Clin Apher
Pays: United States
ID NLM: 8216305

Informations de publication

Date de publication:
Dec 2023
Historique:
revised: 01 08 2023
received: 13 04 2023
accepted: 22 08 2023
pubmed: 14 9 2023
medline: 14 9 2023
entrez: 14 9 2023
Statut: ppublish

Résumé

Therapeutic plasma exchange (TPE) removes both pathologic and protective immunoglobulins (Ig). SARS-CoV-2 immunity is partially mediated by anti-SARS-CoV-2 spike antibodies (SAb), which impair viral host-cell invasion. Nonetheless, the systematic effect of TPE on SAb concentration and SARS-CoV-2 immunity is unknown. Paired plasma waste specimens from the first (first-TPE) and last (last-TPE) TPE treatment were collected from 9 patients between July 21, 2021 and March 1, 2022. The effects of TPE on Ig levels were assessed by quantitatively comparing the SAb, total IgG, and total IgM levels first-/last-TPE treatment. Complementary qualitative assessment for these changes was achieved via protein electrophoresis (PEP) and immunofixation (IFE). A retrospective review was performed to investigate the incidence of new SARS-CoV-2 infections following TPE v. other treatment at the same outpatient apheresis/infusion center during the same time frame. Median SAb levels between the first- and last-TPE waste specimens decreased significantly from 424.6 AU/mL to 17.0 AU/mL (P = 0.004). Concordantly, PEP and IFE analysis demonstrated broad Ig decreases. Cumulative incidence of subsequent COVID-19 diagnosis at 30, 90, and 180 days post-procedure did not differ between the TPE v. other treatment groups (n = 709 total patients). TPE significantly reduced SAb levels, a marker of SARS-CoV-2 immunity, but did not appear to provoke increased incidence of COVID-19 infections. Further investigation of the kinetics of TPE-mediated SAb decrease and post-TPE recovery are warranted.

Sections du résumé

BACKGROUND BACKGROUND
Therapeutic plasma exchange (TPE) removes both pathologic and protective immunoglobulins (Ig). SARS-CoV-2 immunity is partially mediated by anti-SARS-CoV-2 spike antibodies (SAb), which impair viral host-cell invasion. Nonetheless, the systematic effect of TPE on SAb concentration and SARS-CoV-2 immunity is unknown.
METHODS METHODS
Paired plasma waste specimens from the first (first-TPE) and last (last-TPE) TPE treatment were collected from 9 patients between July 21, 2021 and March 1, 2022. The effects of TPE on Ig levels were assessed by quantitatively comparing the SAb, total IgG, and total IgM levels first-/last-TPE treatment. Complementary qualitative assessment for these changes was achieved via protein electrophoresis (PEP) and immunofixation (IFE). A retrospective review was performed to investigate the incidence of new SARS-CoV-2 infections following TPE v. other treatment at the same outpatient apheresis/infusion center during the same time frame.
RESULTS RESULTS
Median SAb levels between the first- and last-TPE waste specimens decreased significantly from 424.6 AU/mL to 17.0 AU/mL (P = 0.004). Concordantly, PEP and IFE analysis demonstrated broad Ig decreases. Cumulative incidence of subsequent COVID-19 diagnosis at 30, 90, and 180 days post-procedure did not differ between the TPE v. other treatment groups (n = 709 total patients).
CONCLUSIONS CONCLUSIONS
TPE significantly reduced SAb levels, a marker of SARS-CoV-2 immunity, but did not appear to provoke increased incidence of COVID-19 infections. Further investigation of the kinetics of TPE-mediated SAb decrease and post-TPE recovery are warranted.

Identifiants

pubmed: 37706521
doi: 10.1002/jca.22087
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

721-726

Subventions

Organisme : Funding provided by Women in Medicine and Science Mentorship Seed Award, Tufts Medical Center

Informations de copyright

© 2023 Wiley Periodicals LLC.

Références

Padmanabhan A, Connelly-Smith L, Aqui N, et al. Guidelines on the use of therapeutic apheresis in clinical practice-evidence-based approach from the writing Committee of the American Society for apheresis: the eighth special issue. J Clin Apher. 2019;34(3):171-354.
Webb JAC. Therapeutic apheresis. In: Cohn C, Delaney M, Johnson S, Katz L, eds. AABB Technical Manual. 20th ed. AABB; Bethesda, MD; 2020:705-735.
Guptill JT, Juel VC, Massey JM, et al. Effect of therapeutic plasma exchange on immunoglobulins in myasthenia gravis. Autoimmunity. 2016;49(7):472-479.
Jackson CB, Farzan M, Chen B, et al. Mechanisms of SARS-CoV-2 entry into cells. Nat Rev Mol Cell Biol. 2022;23(1):3-20.
Zost SJ, Gilchuk P, Case JB, et al. Potently neutralizing and protective human antibodies against SARS-CoV-2. Nature. 2020;584(7821):443-449.
Turner JS, Kim W, Kalaidina E, et al. SARS-CoV-2 infection induces long-lived bone marrow plasma cells in humans. Nature. 2021;595(7867):421-425.
Berkman EM, Orlin JB. Use of plasmapheresis and partial plasma exchange in the management of patients with cryoglobulinemia. Transfusion. 1980;20(2):171-178.
Sette A, Crotty S. Adaptive immunity to SARS-CoV-2 and COVID-19. Cell. 2021;184(4):861-880.
Stahl K, Bode C, David S. First do no harm-beware the risk of therapeutic plasma exchange in severe COVID-19. Crit Care. 2020;24(1):363.
Keith P, Day M, Perkins L, et al. A novel treatment approach to the novel coronavirus: an argument for the use of therapeutic plasma exchange for fulminant COVID-19. Crit Care. 2020 Apr 2;24(1):128.
Shokouhi S, Barati S, Kazeminia N, et al. Evaluating the elimination status of medications used for COVID-19 during hemoperfusion and therapeutic plasma exchange: a review. Int Immunopharmacol. 2021;97:107707.
Bertram S, Pfab T, Albert C, et al. Low-density lipoprotein apheresis is associated with removal of SARS-CoV-2 antibodies. Ther Apher Dial. 2022;26(6):1289-1295.
Gaggl M, Aschauer C, Aigner C, et al. SARS-CoV-2 IgG spike protein antibody response in mRNA-1273 Moderna vaccinated patients on maintenance immunoapheresis-a cohort study. Front Immunol. 2022;13:969193.
Ahmed S, Mehta P, Paul A, et al. Postvaccination antibody titres predict protection against COVID-19 in patients with autoimmune diseases: survival analysis in a prospective cohort. Ann Rheum Dis. 2022;81(6):868-874.
Steensels D, Pierlet N, Penders J, et al. Comparison of SARS-CoV-2 antibody response following vaccination with BNT162b2 and mRNA-1273. JAMA. 2021;326(15):1533-1535.

Auteurs

Jensyn Cone Sullivan (J)

Department of Pathology and Laboratory Medicine, Tufts Medical Center, Boston, Massachusetts, USA.

Steven E Conklin (SE)

Department of Pathology and Laboratory Medicine, Tufts Medical Center, Boston, Massachusetts, USA.
Department of Anatomic & Clinical Pathology, Tufts University School of Medicine, Boston, Massachusetts, USA.

Stephanie Conrad (S)

Department of Pathology and Laboratory Medicine, Tufts Medical Center, Boston, Massachusetts, USA.

Coby Horowitz (C)

Department of Pathology and Laboratory Medicine, Tufts Medical Center, Boston, Massachusetts, USA.

Mark Diethelm (M)

Department of Pathology and Laboratory Medicine, Tufts Medical Center, Boston, Massachusetts, USA.

Raymond Comenzo (R)

Department of Pathology and Laboratory Medicine, Tufts Medical Center, Boston, Massachusetts, USA.

Classifications MeSH