ClinicalTrials.Veeva

Menu

Interleukin-8 Level in Packed Red Blood Cells

A

Assiut University

Status

Not yet enrolling

Conditions

Packed Red Blood Cells

Treatments

Other: ELISA

Study type

Observational

Funder types

Other

Identifiers

NCT06530160
Interleukin-8 in packed Rbcs

Details and patient eligibility

About

  1. To compare level of interleukin-8 between leukodepleted and non-leukodepleted packed red blood cells.
  2. To show the effect of filtration of packed red blood cells on the level of inflammatory interleukin-8.

Full description

The term cytokine was proposed by Stanley Cohen in 1974 and refers to peptides, proteins, and glycoproteins which play a role in controlling the survival/death of cells, their growth and differentiation as well as the effector functions in tissues and immune cells.

The cytokines are small cell-signaling protein molecules with several functions,e.g.: Intracrine, Autocrine and Intercrine actions (1).

They are synthesized by different immune cells, mainly by T cells, neutrophils and macrophages, which are responsible to promote and regulate immune response (i.e. activity, differentiation, proliferation and production of cells and other cytokines) (2).

Cytokines are described as being pro-inflammatory or antiinflammatory, both of which accumulate in blood products during storage mainly as a result of damaged leucocytes. The accumulation of pro-inflammatory cytokines, is regarded as one of the major causative factors For Transfusion-Associated Adverse Reactions (TAARs), particularly Febrile Non-Haemolytic Transfusion Reactions (FNHTRs) and Transfusion-Related Immunomodulation (TRIM). In addition, the transfusion of blood products containing cytokines has been associated with transfusion-induced systemic inflammation in patients with pre-activated endothelial cells (3).

Interleukin-8 (also known as neutrophil-activating peptide 1) is recognized as a potent effector of neutrophil functions. Several different cell types that contact blood, namely T lymphocytes, monocytes, and endothelial cells, secrete this polypeptide following stimulation by cytokines, or lipopolysaccharide (4).

Interleukin-8 (IL-8), a cytokine with chemotactic and activating properties for neutrophils, has recently been isolated, cloned, and expressed.5 IL-8 is produced by monocytes in response to lipopolysaccharide (LPS), tumor necrosis factor-α (TNF-α), and IL-1;6 and has been implicated in the pathogenesis of acute lung injury. Therefore, we hypothesized that IL-8 may be a mediator of the pathologic events in hemolytic transfusion reaction (HTR), and designed an in vitro model of red blood cell (RBC) incompatibility to investigate the possible role of IL-8 in this setting (5).

Leukoreduction (LR) is a potential means of preventing cytokine production (6).

Thus reducing the white blood cell (WBC) content (leukodepletion) in cellular blood components to a significant level has a direct impact on reducing the incidence of many adverse effects of transfusion-associated with leukocytes and cytokines present in higher levels in non leukodepleted blood component (7).

Enrollment

82 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • In total, 82 donors fulfilling all general criteria for blood donation, different blood groups and socioeconomic backgrounds, males and females belonging to this geographical area.

Exclusion criteria

  • Donors not fulfilling all general criteria for blood donation according to World Health Organization:
  • Age between 18 and 65
  • Weight at least 50 kg
  • Haemoglobin not less than 13 g/dl in males and 12 g/dl in females
  • must be in good health at the time of donation
  • Cannot donate if have a cold, flu, sore throat, cold sore, stomach bug or any other infection.
  • Have ever had a positive test for HIV (AIDS virus)
  • It is not advisable to donate blood while Breast-feeding

Trial contacts and locations

0

Loading...

Central trial contact

Rania Mohamed Bakry; Wesam Ashraf Soliman

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems