Search In this Thesis
   Search In this Thesis  
العنوان
Assessment of serum Inhibitory Leucocyte Immunoglobulin-Like Receptor B 4 (LILRB4) level in Adult Egyptian Patients with Acute Lymphoblastic Leukaemia (ALL) and its prognostic value/
المؤلف
Saad,Mohamed Ali Soliman
هيئة الاعداد
باحث / محمد علي سليمان سعد
مشرف / محمد عثمان عزازي
مشرف / محمد محمود متولي موسى
مشرف / هايدي سيد محمد
مشرف / نور الهدى حسين عبد الله
تاريخ النشر
2022
عدد الصفحات
178.p:
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
الطب الباطني
تاريخ الإجازة
1/1/2022
مكان الإجازة
جامعة عين شمس - كلية الطب - Internal Medicine
الفهرس
Only 14 pages are availabe for public view

from 178

from 178

Abstract

ABSTRACT
Background: LILRBs are immunological checkpoint factors because their immune-suppressive effect is comparable to that of CTLA4 and PD-1. LILRBs and a similar ITIM-containing receptor LAIR1 are expressed on and promote tumour growth in haematological and solid cancer cells. Aim: to measure serum LILRB 4 level in the peripheral blood of Egyptian patients with acute lymphoblastic leukaemia and correlating it with clinical outcome and prognosis of the disease. Subject and Methods: This study was conducted at Ain-Shams University Hospitals, division of Clinical Haematology and Oncology-department of Internal Medicine on 60 patients. Results: Serum LILRB4 level was statistically significant higher in ALL patients than healthy controls. LILRB4 serum level was statistically significant higher in patients who developed relapse than those who did not develop relapse. Serum LILRB4 level was statistically significant lower in patients who died than those who survived during induction. LILRB4 serum level was statistically significant higher in patients who died by ARDS and sepsis than those who died by COVID infection. Conclusion: LILRB4 level was statistically significant higher in ALL patients than healthy controls. ALL patients who received Dana-Farber protocol of treatment have statistically significant lower serum LILRB4 level than ALL patients who received hyper-CVAD and CALGB protocol