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Open Access

Alterations in Innate Immune Cells During the Progression of Systemic Autoimmune Rheumatic Diseases

Carmen Ucciferri, Carol Nassar, Sindhu Johnson, Zahi Touma, Zareen Ahmad, Dennisse Bonilla, Andrea Knight, Linda Hiraki, Arthur Bookman and Joan Wither
The Journal of Rheumatology August 2026, 53 (Suppl 1) 78-79; DOI: https://doi.org/10.3899/jrheum.2026-0447.66
Carmen Ucciferri
Schroeder Arthritis Institute, Toronto
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Carol Nassar
Schroeder Arthritis Institute, Toronto
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Sindhu Johnson
Division of Rheumatology, Schroeder Arthritis Institute, University Health Network; Division of Rheumatology, Mount Sinai Hospital; Toronto Scleroderma Program, Toronto
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Zahi Touma
Division of Rheumatology, Schroeder Arthritis Institute, University Health Network; University of Toronto Lupus Clinic, Toronto
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Zareen Ahmad
Division of Rheumatology, Mount Sinai Hospital; Toronto Scleroderma Program, Toronto
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Dennisse Bonilla
Division of Rheumatology, Schroeder Arthritis Institute, University Health Network; University of Toronto Lupus Clinic, Toronto
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Andrea Knight
Division of Rheumatology, Hospital for Sick Children, Toronto
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Linda Hiraki
Division of Rheumatology, Hospital for Sick Children, Toronto
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Arthur Bookman
Division of Rheumatology, Western Hospital, University Health Network, Toronto
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Joan Wither
Division of Rheumatology, Schroeder Arthritis Institute, University Health Network; Schroeder Arthritis Institute Krembil Research Institute, Toronto
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  • Innate immune cells during the progression of SARD. A) Feature plots from CITE-Seq of monocytes and DCs shotting HSPA1A (HSP70), CD52 (CD52) and HLA-DRB5 (MHC Class II). B) Spectral flow cytometry showing representative results from classical monocytes tor HLA-DR and CD52 protein expression. C) Gene expression of HSPA1A (HSP70) by RT-qPCR and soluble HSP70 (sHSP70) concentration by supernatant ELISAs measured in a THP-1 monocyte cell line. Cells were heat shocked (43°C for 1h) and subsequently rested for 6h, 12h, 18h, 24h before collection. E) Heat shocked THP-1 cells were rested for 12h and used for cytospin with subsequent immunofluorescence staining with DAPI for cell nuclei and HSP70 (scale bar = 50 μm). E) Plasma ELISAs for soluble HSP70 in patient cohort. Data was analyzed using a Kruskal-Wallis test with Dunn post hoe and Bonferroni correction (* = p-value < 0.05).
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    Figure 1.

    Innate immune cells during the progression of SARD. A) Feature plots from CITE-Seq of monocytes and DCs shotting HSPA1A (HSP70), CD52 (CD52) and HLA-DRB5 (MHC Class II). B) Spectral flow cytometry showing representative results from classical monocytes tor HLA-DR and CD52 protein expression. C) Gene expression of HSPA1A (HSP70) by RT-qPCR and soluble HSP70 (sHSP70) concentration by supernatant ELISAs measured in a THP-1 monocyte cell line. Cells were heat shocked (43°C for 1h) and subsequently rested for 6h, 12h, 18h, 24h before collection. E) Heat shocked THP-1 cells were rested for 12h and used for cytospin with subsequent immunofluorescence staining with DAPI for cell nuclei and HSP70 (scale bar = 50 μm). E) Plasma ELISAs for soluble HSP70 in patient cohort. Data was analyzed using a Kruskal-Wallis test with Dunn post hoe and Bonferroni correction (* = p-value < 0.05).

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The Journal of Rheumatology: 53 (Suppl 1)
The Journal of Rheumatology
Vol. 53, Issue Suppl 1
1 Aug 2026
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Alterations in Innate Immune Cells During the Progression of Systemic Autoimmune Rheumatic Diseases
Carmen Ucciferri, Carol Nassar, Sindhu Johnson, Zahi Touma, Zareen Ahmad, Dennisse Bonilla, Andrea Knight, Linda Hiraki, Arthur Bookman, Joan Wither
The Journal of Rheumatology Aug 2026, 53 (Suppl 1) 78-79; DOI: 10.3899/jrheum.2026-0447.66

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Alterations in Innate Immune Cells During the Progression of Systemic Autoimmune Rheumatic Diseases
Carmen Ucciferri, Carol Nassar, Sindhu Johnson, Zahi Touma, Zareen Ahmad, Dennisse Bonilla, Andrea Knight, Linda Hiraki, Arthur Bookman, Joan Wither
The Journal of Rheumatology Aug 2026, 53 (Suppl 1) 78-79; DOI: 10.3899/jrheum.2026-0447.66
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