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Immunology Testing

Immune Deficiency Panel 1 Test

The Immune Deficiency Panel 1 Test evaluates key immune components to help diagnose conditions where the immune system may not function properly. This test measures CD3, CD4, CD8, CD19, and CD16+/CD56 levels.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Two whole blood tubes: one Lavender Top (EDTA) and one Green Top (Sodium Heparin). Minimum volume: 2 mL per tube.
Results
Confirm with the laboratory before booking.
Preparation
No special preparation is required for this test. However, please inform the laboratory of any medications you are currently taking.
Test priceKSh 17,000

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the Immune Deficiency Panel 1 Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Recurrent infections
  • ✓Family history of immunodeficiency
  • ✓Unexplained fatigue or malaise
  • ✓Symptoms suggestive of autoimmune disease
  • ✓Evaluation of immune status before major surgery or immunosuppressive therapy
  • ✓Monitoring response to treatment for immunodeficiency
02

In plain language

What this test helps you understand

This test helps evaluate immune system function by measuring key lymphocyte populations. It aids in the diagnosis and monitoring of various immunodeficiency disorders and conditions affecting immune cell counts.
The Immune Deficiency Panel 1 Test is a diagnostic tool used to assess the function of your immune system. It helps identify potential immunodeficiency states, which can make individuals more susceptible to infections and other health issues. Understanding your immune health is important for timely medical care. This test measures specific types of immune cells, providing a detailed look at your immune status. It is recommended for individuals experiencing recurrent infections, those with a family history of immunodeficiency, or those with unexplained fatigue or symptoms suggestive of autoimmune conditions. Early detection through this test can guide appropriate treatment and preventive care strategies. Results will be interpreted by a healthcare professional to determine the next steps.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationNo special preparation is required for this test. However, please inform the laboratory of any medications you are currently taking.
SampleTwo whole blood tubes: one Lavender Top (EDTA) and one Green Top (Sodium Heparin). Minimum volume: 2 mL per tube.
MethodologyFlow cytometry is used to measure the percentage and absolute counts of specific immune cell populations (CD3, CD4, CD8, CD19, CD16+/CD56) in the blood sample.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
Results may be affected by recent infections, inflammation, certain medications, or other medical conditions. This test provides a snapshot of immune cell counts at the time of collection and may not reflect long-term immune function. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

This test measures the levels of specific types of white blood cells (lymphocytes) including CD3, CD4, CD8, CD19, and CD16+/CD56, which are important components of the immune system.
This test is often recommended if you have frequent infections, a family history of immune problems, or symptoms that suggest your immune system might not be working correctly.
The sample is collected via a blood draw. Two tubes of blood will be needed: one Lavender Top (EDTA) and one Green Top (Sodium Heparin).
Turnaround time varies. Please contact the laboratory for specific details regarding this test.
No fasting is required for this test.
Samples should be shipped immediately at room temperature (18°C to 22°C). Do not refrigerate or freeze.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

Explore partnerships
09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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