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A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19

Yıl 2022, Cilt: 85 Sayı: 3, 291 - 295, 06.07.2022
https://doi.org/10.26650/IUITFD.1079629

Öz

Objective: During viral infections, antibody production of B cells are critical for protective immunity. It is known that the COVID-19 disease has a milder course in children. It is crucial to evaluate the causes of this situation from a pediatrician’s perspective to determine the treatment goals of the disease. We aimed to examine the flow cytometric changes in B cells and subtypes observed in children diagnosed with the COVID-19 infection.
Materials and Methods: This is a prospective cohort study including 22 children aged 0-18 who had been diagnosed with COVID-19. CD19+B cells, CD27-IgD+ naive B, CD21low immature B, CD21lowCD38low active B, CD27-IgD- double-negative B, CD27- non-memory B, CD27+ memory B, CD27+IgD- switched memory B, and CD27+IgD+ non-switched memory B cells were studied using flow cytometry.
Results: B cells counts decreased as a percentage in the 2-5 years age group and the 10-16 age group as an absolute number. Naive and non-memory B cell frequencies increased in the 5-10 years old and over 16 years old groups. Double negative B cells were normal in all age groups. Non-memory B cells increased in the 5-10 and over 16 years old groups, whereas memory B cells decreased. In all groups, switched memory B cells decreased. Non-switched memory B cell counts were within reference ranges in all groups except for the over 16 years group.
Conclusion: Although the decrease in B cell count is associated with the severity of the disease, naive B cell subgroups did not decrease in the pediatric patients included in the study. All groups showed increased switched memory B cell counts, in accordance with the literature. Unlike adults, naive B cells, non-switched memory B cells, and double-negative B cells were normal in children.

Kaynakça

  • 1. Baker D, Roberts CA, Pryce G, Kang AS, Marta M, Reyes S, et al. COVID-19 vaccine-readiness for anti-CD20-depleting therapy in autoimmune diseases. Clin Exp Immunol 2020;202(2):149-61. [CrossRef] google scholar
  • 2. Chiappelli F. COVID-19 Immunopathology & Immunotherapy. Bioinformation 2020;16(3):219-22. [CrossRef] google scholar
  • 3. Comans-Bitter WM, De Groot R, Van den Beemd R, Neijens HJ, Hop WCJ, Groeneveld K, et al. Immunophenotyping of blood lymphocytes in childhood: Reference values for lymphocyte subpopulations. J Pediatr 1997;130(3):388-93. [CrossRef] google scholar
  • 4. Deng Z, Zhang M, Zhu T, Zhili N, Liu Z, Xiang R, et al. Dynamic changes in peripheral blood lymphocyte subsets in adult patients with COVID-19. Int J Infect Dis 2020;98:353-8. [CrossRef] google scholar
  • 5. Devogelaere J, D’hooghe MB, Vanderhauwaert F, D’haeseleer M. Coronavirus disease 2019: favorable outcome in an immunosuppressed patient with multiple sclerosis. Neurol Sci 2020;41(8):1981-3. [CrossRef] google scholar
  • 6. He R, Lu Z, Zhang L, Fan T, Xiong R, Shen X, et al. The clinical course and its correlated immune status in COVID-19 pneumonia. J Clin Virol 2020;127:104361. [CrossRef] google scholar
  • 7. Huang W, Berube J, McNamara M, Saksena S, Hartman M, Arshad T, et al. Lymphocyte Subset Counts in COVID-19 Patients: A Meta-Analysis. Cytom Part A 2020;97(8):772-6. [CrossRef] google scholar
  • 8. Kebudi R, Kurucu N, Tuğcu D, Hacısalihoğlu Ş, Fışgın T, Ocak S, et al. COVID-19 infection in children with cancer and stem cell transplant recipients in Turkey: A nationwide study. Pediatr Blood Cancer 2021;68(6):e28915. [CrossRef] google scholar
  • 9. Li H, Chen K, Liu M, Xu H, Xu Q. The profile of peripheral blood lymphocyte subsets and serum cytokines in children with 2019 novel coronavirus pneumonia. J Infect 2020;81(1):115-20. [CrossRef] google scholar
  • 10. Liu J, Li S, Liu J, Liang B, Wang X, Wang H, et al. Longitudinal characteristics of lymphocyte responses and cytokine profiles in the peripheral blood of SARS-CoV-2 infected patients. EBioMedicine 2020;55:1027633. [CrossRef] google scholar
  • 11. Machura E, Mazur B, Pienişzek W, Karczewska K. Expression of naive/memory (CD45RA/CD45RO) markers by peripheral blood CD4 + and CD8 + T cells in children with asthma. Arch Immunol Ther Exp (Warsz) 2008;56(1):55-62. [CrossRef] google scholar
  • 12. Mathew D, Giles JR, Baxter AE, Oldridge DA, Greenplate AR, Wu JE, et al. Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications. Science 2020;369(6508):eabc8511. [CrossRef] google scholar
  • 13. Melek Arsoy HE, Özdemir Ö. Mysterious Side of COVID-19 Pandemic: Children. Istanbul Med J 2020;21(4):242-57. [CrossRef] google scholar
  • 14. Nielsen S, Fang Y, Jackson K, Hoh R, Röltgen K, Stevens B, et al. Human B cell clonal expansion and convergent antibody responses to SARS-CoV-2. Cell Host Microbe 2020;28(4):516-525.e5. [CrossRef] google scholar
  • 15. Orhan MF, Büyükavcı M. COVID-19’un Tanı ve Tedavi Sürecinde Hematolojik Parametreler. J Biotechnol Strateg Heal Res 2020;4:123-7. [CrossRef] google scholar
  • 16. Özdemir Ö. Coronavirus Disease 2019 (COVID-19): Diagnosis and Management (narrative review). Erciyes Med J 2020;42(3):242-7. [CrossRef] google scholar
  • 17. Özdemir Ö. İmmün sistemin COVID-19 hastalığındaki rolü: Patogenezden tedaviye. Bostancı İ, editör. Çocuk Sağlığında SARSCoV- 2 (COVID-19). 1. Baskı. Ankara: Türkiye Klinikleri; 2020. p.14-21. google scholar
  • 18. Özdemir Ö, Erkun O. Solving puzzle of the immunopathogenesis for management of COVID-19 disease. MOJ Immunol 2020;7(1):13-5. google scholar
  • 19. Schatorje EJH, Gemen EFA, Driessen GJA, Leuvenink J, van Hout RWNM, et al. Age-matched reference values for B-lymphocyte subpopulations and CVID classifications in children. Scand J Immunol 2011;74(5):502-10. [CrossRef] google scholar
  • 20. Schatorje EJH, Gemen EFA, Driessen GJA, Leuvenink J, van Hout RWNM, de Vries E. Paediatric reference values for the peripheral T cell compartment. Scand J Immunol 2012;75(4):436-44. [CrossRef] google scholar
  • 21. Shearer WT, Rosenblatt HM, Gelman RS, Oyomopito R, Plaeger S, Stiehm ER, et al. Lymphocyte subsets in healthy children from birth through 18 years of age: The Pediatric AIDS Clinical Trials Group P1009 study. J Allergy Clin Immunol 2003;112(5):973-80. [CrossRef] google scholar
  • 22. Tan M, Liu Y, Zhou R, Deng X, Li F, Liang K, et al. Immunopathological characteristics of coronavirus disease 2019 cases in Guangzhou, China. Immunology 2020;160(3):261-8. [CrossRef] google scholar
  • 23. Wang F, Hou H, Luo Y, Tang G, Wu S, Huang M, et al. The laboratory tests and host immunity of COVID-19 patients with different severity of illness. JCI Insight 2020;5(10):e137799. [CrossRef] google scholar
  • 24. Wang F, Nie J, Wang H, Zhao Q, Xiong Y, Deng L, et al. Characteristics of peripheral lymphocyte subset alteration in COVID-19 Pneumonia. J Infect Dis 2020;221(11):11762-9. [CrossRef] google scholar
  • 25. Wen W, Su W, Tang H, Le W, Zhang X, Zheng Y, et al. Immune cell profiling of COVID-19 patients in the recovery stage by single-cell sequencing. Cell Discov 2020;6(1):31. [CrossRef] google scholar

COVİD-19 TANISI ALAN ÇOCUKLARIN B LENFOSİT HÜCRELERİNİN VE ALT GRUPLARININ AKIŞ SİTOMETRİK DEĞERLENDİRİLMESİ

Yıl 2022, Cilt: 85 Sayı: 3, 291 - 295, 06.07.2022
https://doi.org/10.26650/IUITFD.1079629

Öz

Amaç: Viral enfeksiyonlar sırasında B hücrelerinin antikor üretimi, koruyucu bağışıklık için kritiktir. Çocuklarda COVID-19 hastalığının daha hafif seyrettiği bilinmektedir. Bu durumun nedenlerini çocuk doktoru gözüyle değerlendirmek, hastalığın tedavi hedeflerini belirlemek açısından çok önemlidir. COVID-19 enfeksiyonu tanısı alan çocuklarda gözlenen B hücre ve alt tiplerinde akım sitometrik değişiklikleri incelemeyi amaçladık.
Gereç ve Yöntem: Çalışmamız 0-18 yaş arası COVID-19 teşhisi konulan 22 çocuğu içeren prospektif kohort bir araştırmadır. CD19+B hücreleri, CD27-IgD+ saf B, CD21düşük olgunlaşmamış B, CD21düşükCD38düşük aktif B, CD27-IgD- çift negatif B, CD27- bel- lek B, CD27+ bellek B, CD27+IgD- dönüşmüş (switched) bellek B, CD27+IgD+ dönüşmemiş (non-switched) bellek B hücreleri akış sitometrisi ile incelenmiştir.
Bulgular: B hücre sayısı 2-5 yaş grubunda yüzde olarak, 10-16 yaş grubunda ise mutlak sayı olarak azaldı. 5-10 yaş ve 16 yaş üstü gruplarda naif ve hafıza dışı B hücrelerinin oranları arttı. Çift negatif B hücreleri tüm yaş gruplarında normaldi. Bellek dışı B hücreleri 5-10 yaş arasında ve 16 yaş üzerinde artarken, aynı gruplarda bellek B hücreleri azaldı. Dönüşmüş bellek B hücreleri tüm yaş gruplarında azaldı. Dönüşmemiş bellek B hücreleri, 16 yaşın üzerinde azaldı ve diğer tüm yaş gruplarında normal görünüyordu.
Sonuç: B hücre sayısındaki azalma hastalığın şiddeti ile ilişkili olmasına rağmen, çalışmaya dâhil edilen çocuk hastalarımızda naif B hücre alt gruplarında azalma olmadı. Literatüre uygun olarak tüm gruplarda dönüşmüş bellek B hücreleri arttı. Çocuklarda yetişkinlerden farklı olarak naif B hücreleri, dönüşmemiş bellek B hücreleri ve çift negatif B hücreleri normaldi.

Kaynakça

  • 1. Baker D, Roberts CA, Pryce G, Kang AS, Marta M, Reyes S, et al. COVID-19 vaccine-readiness for anti-CD20-depleting therapy in autoimmune diseases. Clin Exp Immunol 2020;202(2):149-61. [CrossRef] google scholar
  • 2. Chiappelli F. COVID-19 Immunopathology & Immunotherapy. Bioinformation 2020;16(3):219-22. [CrossRef] google scholar
  • 3. Comans-Bitter WM, De Groot R, Van den Beemd R, Neijens HJ, Hop WCJ, Groeneveld K, et al. Immunophenotyping of blood lymphocytes in childhood: Reference values for lymphocyte subpopulations. J Pediatr 1997;130(3):388-93. [CrossRef] google scholar
  • 4. Deng Z, Zhang M, Zhu T, Zhili N, Liu Z, Xiang R, et al. Dynamic changes in peripheral blood lymphocyte subsets in adult patients with COVID-19. Int J Infect Dis 2020;98:353-8. [CrossRef] google scholar
  • 5. Devogelaere J, D’hooghe MB, Vanderhauwaert F, D’haeseleer M. Coronavirus disease 2019: favorable outcome in an immunosuppressed patient with multiple sclerosis. Neurol Sci 2020;41(8):1981-3. [CrossRef] google scholar
  • 6. He R, Lu Z, Zhang L, Fan T, Xiong R, Shen X, et al. The clinical course and its correlated immune status in COVID-19 pneumonia. J Clin Virol 2020;127:104361. [CrossRef] google scholar
  • 7. Huang W, Berube J, McNamara M, Saksena S, Hartman M, Arshad T, et al. Lymphocyte Subset Counts in COVID-19 Patients: A Meta-Analysis. Cytom Part A 2020;97(8):772-6. [CrossRef] google scholar
  • 8. Kebudi R, Kurucu N, Tuğcu D, Hacısalihoğlu Ş, Fışgın T, Ocak S, et al. COVID-19 infection in children with cancer and stem cell transplant recipients in Turkey: A nationwide study. Pediatr Blood Cancer 2021;68(6):e28915. [CrossRef] google scholar
  • 9. Li H, Chen K, Liu M, Xu H, Xu Q. The profile of peripheral blood lymphocyte subsets and serum cytokines in children with 2019 novel coronavirus pneumonia. J Infect 2020;81(1):115-20. [CrossRef] google scholar
  • 10. Liu J, Li S, Liu J, Liang B, Wang X, Wang H, et al. Longitudinal characteristics of lymphocyte responses and cytokine profiles in the peripheral blood of SARS-CoV-2 infected patients. EBioMedicine 2020;55:1027633. [CrossRef] google scholar
  • 11. Machura E, Mazur B, Pienişzek W, Karczewska K. Expression of naive/memory (CD45RA/CD45RO) markers by peripheral blood CD4 + and CD8 + T cells in children with asthma. Arch Immunol Ther Exp (Warsz) 2008;56(1):55-62. [CrossRef] google scholar
  • 12. Mathew D, Giles JR, Baxter AE, Oldridge DA, Greenplate AR, Wu JE, et al. Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications. Science 2020;369(6508):eabc8511. [CrossRef] google scholar
  • 13. Melek Arsoy HE, Özdemir Ö. Mysterious Side of COVID-19 Pandemic: Children. Istanbul Med J 2020;21(4):242-57. [CrossRef] google scholar
  • 14. Nielsen S, Fang Y, Jackson K, Hoh R, Röltgen K, Stevens B, et al. Human B cell clonal expansion and convergent antibody responses to SARS-CoV-2. Cell Host Microbe 2020;28(4):516-525.e5. [CrossRef] google scholar
  • 15. Orhan MF, Büyükavcı M. COVID-19’un Tanı ve Tedavi Sürecinde Hematolojik Parametreler. J Biotechnol Strateg Heal Res 2020;4:123-7. [CrossRef] google scholar
  • 16. Özdemir Ö. Coronavirus Disease 2019 (COVID-19): Diagnosis and Management (narrative review). Erciyes Med J 2020;42(3):242-7. [CrossRef] google scholar
  • 17. Özdemir Ö. İmmün sistemin COVID-19 hastalığındaki rolü: Patogenezden tedaviye. Bostancı İ, editör. Çocuk Sağlığında SARSCoV- 2 (COVID-19). 1. Baskı. Ankara: Türkiye Klinikleri; 2020. p.14-21. google scholar
  • 18. Özdemir Ö, Erkun O. Solving puzzle of the immunopathogenesis for management of COVID-19 disease. MOJ Immunol 2020;7(1):13-5. google scholar
  • 19. Schatorje EJH, Gemen EFA, Driessen GJA, Leuvenink J, van Hout RWNM, et al. Age-matched reference values for B-lymphocyte subpopulations and CVID classifications in children. Scand J Immunol 2011;74(5):502-10. [CrossRef] google scholar
  • 20. Schatorje EJH, Gemen EFA, Driessen GJA, Leuvenink J, van Hout RWNM, de Vries E. Paediatric reference values for the peripheral T cell compartment. Scand J Immunol 2012;75(4):436-44. [CrossRef] google scholar
  • 21. Shearer WT, Rosenblatt HM, Gelman RS, Oyomopito R, Plaeger S, Stiehm ER, et al. Lymphocyte subsets in healthy children from birth through 18 years of age: The Pediatric AIDS Clinical Trials Group P1009 study. J Allergy Clin Immunol 2003;112(5):973-80. [CrossRef] google scholar
  • 22. Tan M, Liu Y, Zhou R, Deng X, Li F, Liang K, et al. Immunopathological characteristics of coronavirus disease 2019 cases in Guangzhou, China. Immunology 2020;160(3):261-8. [CrossRef] google scholar
  • 23. Wang F, Hou H, Luo Y, Tang G, Wu S, Huang M, et al. The laboratory tests and host immunity of COVID-19 patients with different severity of illness. JCI Insight 2020;5(10):e137799. [CrossRef] google scholar
  • 24. Wang F, Nie J, Wang H, Zhao Q, Xiong Y, Deng L, et al. Characteristics of peripheral lymphocyte subset alteration in COVID-19 Pneumonia. J Infect Dis 2020;221(11):11762-9. [CrossRef] google scholar
  • 25. Wen W, Su W, Tang H, Le W, Zhang X, Zheng Y, et al. Immune cell profiling of COVID-19 patients in the recovery stage by single-cell sequencing. Cell Discov 2020;6(1):31. [CrossRef] google scholar
Toplam 25 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Sağlık Kurumları Yönetimi
Bölüm ARAŞTIRMA
Yazarlar

Mehmet Fatih Orhan 0000-0001-8081-6760

Öner Özdemir 0000-0002-5338-9561

Gülay Trak 0000-0002-4120-7249

Yayımlanma Tarihi 6 Temmuz 2022
Gönderilme Tarihi 26 Şubat 2022
Yayımlandığı Sayı Yıl 2022 Cilt: 85 Sayı: 3

Kaynak Göster

APA Orhan, M. F., Özdemir, Ö., & Trak, G. (2022). A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19. Journal of Istanbul Faculty of Medicine, 85(3), 291-295. https://doi.org/10.26650/IUITFD.1079629
AMA Orhan MF, Özdemir Ö, Trak G. A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19. İst Tıp Fak Derg. Temmuz 2022;85(3):291-295. doi:10.26650/IUITFD.1079629
Chicago Orhan, Mehmet Fatih, Öner Özdemir, ve Gülay Trak. “A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19”. Journal of Istanbul Faculty of Medicine 85, sy. 3 (Temmuz 2022): 291-95. https://doi.org/10.26650/IUITFD.1079629.
EndNote Orhan MF, Özdemir Ö, Trak G (01 Temmuz 2022) A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19. Journal of Istanbul Faculty of Medicine 85 3 291–295.
IEEE M. F. Orhan, Ö. Özdemir, ve G. Trak, “A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19”, İst Tıp Fak Derg, c. 85, sy. 3, ss. 291–295, 2022, doi: 10.26650/IUITFD.1079629.
ISNAD Orhan, Mehmet Fatih vd. “A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19”. Journal of Istanbul Faculty of Medicine 85/3 (Temmuz 2022), 291-295. https://doi.org/10.26650/IUITFD.1079629.
JAMA Orhan MF, Özdemir Ö, Trak G. A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19. İst Tıp Fak Derg. 2022;85:291–295.
MLA Orhan, Mehmet Fatih vd. “A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19”. Journal of Istanbul Faculty of Medicine, c. 85, sy. 3, 2022, ss. 291-5, doi:10.26650/IUITFD.1079629.
Vancouver Orhan MF, Özdemir Ö, Trak G. A FLOW CYTOMETRIC EVALUATION OF B LYMPHOCYTE CELLS AND SUBGROUPS OF CHILDREN DIAGNOSED WITH COVID-19. İst Tıp Fak Derg. 2022;85(3):291-5.

Contact information and address

Addressi: İ.Ü. İstanbul Tıp Fakültesi Dekanlığı, Turgut Özal Cad. 34093 Çapa, Fatih, İstanbul, TÜRKİYE

Email: itfdergisi@istanbul.edu.tr

Phone: +90 212 414 21 61