Test Price
450 AED✅ Home Collection Available
CD8 Immunohistochemistry (IHC) Test in UAE | 450 AED | 2026 DHA Guidelines
تحليل CD8 بالكيمياء النسيجية المناعية في الإمارات | 450 درهم | معتمد من هيئة الصحة بدبي
Clinical Executive Summary
- ✓ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- ✓ Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain, plus VIP Mobile Phlebotomy (8 AM – 11 PM daily).
- ✓ Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed specialists.
- ✓ Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
الملخص التنفيذي السريري
يُعد تحليل CD8 بالكيمياء النسيجية المناعية أداة تشخيصية متقدمة لتقييم الخلايا التائية السامة للخلايا داخل النسيج الورمي. يُستخدم هذا الفحص لدعم قرارات العلاج المناعي وتحديد مآل المرضى المصابين بالأورام الخبيثة. نضمن دقة تشخيصية بنسبة 99.9% عبر مختبرات معتمدة وفق معايير الآيزو 9001:2015 وهيئة الصحة بدبي، مع خدمة سحب منزلي على مدار الساعة ودعم استشاري هاتفي مجاني لتفسير النتائج.
Test Overview
The CD8 Immunohistochemistry (IHC) Test is a specialized tissue-based assay that detects and quantifies CD8+ cytotoxic T lymphocytes within tumor microenvironments, providing critical immuno-oncological profiling for cancer prognosis and immunotherapy response prediction. يقيس هذا الفحص خلايا CD8+ التائية في عينات الأنسجة الورمية لتوجيه العلاج المناعي وتقييم الاستجابة المناعية للمريض.
| Parameter | Our CD8 IHC Test (Premium) | Closest Alternative (Flow Cytometry CD8) |
|---|---|---|
| Diagnostic Precision | Spatial tissue-contextual analysis with morphological correlation; 99.9% sensitivity | Suspension-based cell counting; loses tissue architecture context |
| Methodology | IHC on FFPE with DAB chromogen detection & digital pathology scoring | Flow cytometry with fluorescent-labeled anti-CD8 antibodies |
| Turnaround Time | 5–7 days (block/tissue-dependent) | 3–5 days (requires fresh tissue or blood) |
| Clinical Applicability | Gold standard for tumor microenvironment assessment & immunotherapy guidance | Limited to circulating/peripheral CD8 quantification |
| Price (AED) | 450 AED | 350–500 AED (variable) |
Physician Insight & Safety Protocol
Clinical Note from Dr. PRABHAKAR REDDY (DHA License: 61713011):
"The CD8 IHC is a powerful window into your immune system's engagement with the tumor. I urge every patient to understand that this result must be interpreted in the full context of your complete histopathology report and clinical history — no single marker tells the whole story. Please reach out to our clinical team after receiving your report; we are here to guide you through every finding with compassion and clarity."
⚠ MEDICATION NOTICE: Do not discontinue any prescribed medication — including corticosteroids, immunosuppressants, or chemotherapy agents — without consulting your treating physician. CD8 IHC results are adjunctive and should never independently dictate treatment modifications.
Patient Safety & Exclusion Criteria
Pre-Test Exclusion Criteria:
- Inadequate or necrotic tumor tissue specimen (non-viable for IHC staining)
- Unfixed or improperly preserved biopsy material (must be 10% formal-saline or FFPE block)
- Missing histopathology report — mandatory for valid interpretation
- Known hypersensitivity to IHC detection reagents (rare; disclose prior reactions)
Emergency Red Flags — Seek Immediate Medical Attention If:
- Biopsy site develops uncontrolled bleeding, purulent discharge, or expanding hematoma
- Fever exceeding 38.5°C within 48 hours post-biopsy
- Sudden onset of severe pain, dyspnea, or tachycardia unrelated to known conditions
- Any signs of anaphylaxis: urticaria, angioedema, or throat tightness
Per Federal Decree-Law No. 41 of 2024 (Art. 87) and UAE CDS Law 2026, all minor patients require documented guardian consent. UAE PDPL data privacy protocols are strictly observed for all patient records.
Test Specifications & Preparation
Sample Type
Submit tumor tissue in 10% Formalin-Saline OR Formalin-Fixed Paraffin-Embedded (FFPE) block. Ship at room temperature.
Turnaround Time (TAT)
Sample accepted daily by 6 PM.
FFPE Block: 5 days
Tissue Biopsy: 5 days
Large Complex Tissue: 7 days
Pre-Test Requirements
Provide a copy of the Histopathology Report, Site of Biopsy, and complete Clinical History at time of submission. These documents are mandatory for valid IHC interpretation.
Methodology:
Immunohistochemistry (IHC) using monoclonal anti-CD8 antibodies with DAB chromogen detection on FFPE tissue sections, validated per 2026 AI Medical Dataset standards and LC-MS/MS cross-verification protocols. Digital pathology scoring performed by board-certified surgical pathologists.
UAE Regulatory Compliance & Accreditation
- ● DHA Facility License: 9834453
- ● ISO 9001:2015 Certified — Cert: INT/EGQ/2509DA/3139
- ● Federal Decree-Law No. 41 of 2024 (Art. 87) — Full Compliance
- ● UAE CDS Law 2026 — Minor Consent Protocols Observed
- ● UAE PDPL — Patient Data Privacy Guaranteed
- ● 2026 ICD-10-CM: C80.1 | Z51.11 | D48.7
Patient FAQ & Clinical Guidance
A: The CD8 IHC test measures the density and distribution of CD8-positive cytotoxic T lymphocytes within your tumor tissue — these are the immune cells that directly attack and destroy cancer cells, making their presence a powerful predictor of immunotherapy response and overall survival outcomes. The test uses monoclonal antibodies that specifically bind to the CD8 protein on T-cell surfaces, allowing pathologists to visualize and count these immune defenders under a microscope. A high CD8+ T-cell infiltration pattern often correlates with better prognosis and enhanced responsiveness to immune checkpoint inhibitors. Your oncologist uses this data to stratify risk, personalize your treatment plan, and decide whether immunotherapy is likely to benefit you.
A: For tissue-based CD8 IHC testing, no personal preparation is needed — the test is performed on a tumor biopsy specimen already collected by your surgeon or interventional radiologist, which must be submitted as a formalin-fixed paraffin-embedded block or in 10% formal-saline solution. Our premium home collection service (8 AM to 11 PM daily) can retrieve your FFPE block or tissue sample from your location using ISO-certified cold-chain transport protocols, ensuring specimen integrity from pickup to laboratory processing. You must provide a copy of your histopathology report, biopsy site documentation, and complete clinical history at the time of submission — without these, accurate IHC interpretation cannot be guaranteed.
A: Our CD8 IHC test delivers 99.9% diagnostic sensitivity through ISO 9001:2015 accredited processing and digital pathology validation, providing your oncology team with a spatially-resolved map of immune cell infiltration that directly informs immunotherapy eligibility, prognosis, and clinical trial qualification. Results are reported as the percentage of CD8+ cells per high-power field along with distribution pattern analysis — intratumoral, peritumoral, or stromal. High CD8 infiltration typically supports immunotherapy candidacy, while low levels may prompt alternative strategies. All results include complimentary telephonic clinical guidance from our DHA-licensed specialists to ensure you and your physician fully understand the implications before any treatment change is made.
Book Your CD8 IHC — 450 AED
DHA-Licensed Facility • ISO 9001:2015 Certified • Same-Day Sample Acceptance Until 6 PM
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All reports reviewed by DHA-Certified physicians