Related Experiment Video
Updated: Apr 12, 2026

Murine Kidney Transplant Technique
Published on: October 20, 2015
[Immuknow and long term kidney graft]
Introduction:
The survival of transplanted kidneys has improved over time, but there is an increased risk of neoplastic disease. In the long time follow up, non-melanoma skin cancers (NMSC) are the most frequent diseases and at the time of the occurrence of a NMSC we should evaluate a reduction or a change of IS. From a clinical point of view, the evaluation of immunosuppression is still a problem. The Immuknow assay may be of help in evaluating the immune response of transplanted patients. Here, by means of the ImmKnow assay, we tried to evaluate if long term renal transplant patients with NMSC are more immunosuppressed than patients without NMSC.
Methods:
33 long term kidney transplant patients, 16 with NMSC and 17 without NMSC, were recruited and blood samples were drawn at baseline, 4 months, 8 months and 12 months to check renal function, blood levels of cni and to perform immuknow assay.
Results:
most values of T CD4+ reactivity were comprised between (atp) 225 and 525 ng/ml as for an moderate immunosuppression. No major differences have been observed between the two groups. No correlation with blood level of CNI was detected. T CD4+ activity changed over time for both the groups. 3 patients of the group without NMSC had levels of CD4+ reactivity constantly under (ATP) 225 ng/ml, classified as low per manifacturers definition.
Conclusion:
in our limited experience the measure of cell-mediated immunity by immuknow assay years after transplantation, has not evidenced any significant difference between patients positive for NMSC and negative patients. We observed variation of the CD4 reactivity with time, no correlation with the level of CNI and the useful identification of some cases of low levels of cell reactivity.
Insights
Long-term kidney transplant patients with non-melanoma skin cancer (NMSC) show similar cell-mediated immunity levels compared to those without NMSC. The Immuknow assay did not reveal significant differences in immunosuppression between these groups.
Area of Science:
- Nephrology
- Immunology
- Oncology
Background:
- Kidney transplant survival has improved, but cancer risk, particularly non-melanoma skin cancer (NMSC), increases.
- Evaluating immunosuppression (IS) in long-term transplant patients, especially after NMSC diagnosis, remains challenging.
- The Immuknow assay offers a potential tool for assessing immune response in transplant recipients.
Purpose of the Study:
- To investigate whether long-term kidney transplant patients diagnosed with NMSC exhibit altered levels of immunosuppression compared to those without NMSC.
- To evaluate the utility of the Immuknow assay in differentiating immunosuppression status in kidney transplant recipients with and without NMSC.
Main Methods:
- A cohort of 33 long-term kidney transplant patients (16 with NMSC, 17 without) was studied.
- Blood samples were collected at multiple time points (baseline, 4, 8, 12 months) for renal function, calcineurin inhibitor (CNI) levels, and Immuknow assay.
- The Immuknow assay measures T CD4+ cell reactivity as an indicator of immune response.
Main Results:
- Most patients exhibited moderate immunosuppression, with T CD4+ reactivity between 225-525 ng/ml.
- No significant differences in T CD4+ reactivity were observed between the NMSC and no-NMSC groups.
- No correlation was found between T CD4+ reactivity and blood CNI levels; however, some patients showed persistently low reactivity.
Conclusions:
- The Immuknow assay, in this limited study, did not reveal significant differences in cell-mediated immunity between kidney transplant patients with and without NMSC.
- T CD4+ reactivity varied over time and did not correlate with CNI levels.
- The assay identified some cases with low cell reactivity, warranting further investigation.
Related Concept Videos
Kidney Transplant I: Introduction
Kidney Transplant II: Surgical Procedure
Kidney Transplant III: Nursing Management
Acute Kidney Injury III: Clinical Manifestations
Acute Kidney Injury IV: Diagnostic Studies and Prevention

