Ankylosing SpondylitisInterleukinsNCT07396194
Ankylosing Spondylitis
An observational study of Ankylosing Spondylitis, run by Sohag University.
Trial summary
The goal of this observational study is to measure the serum level of cytokines IL-17, IL-38,IL-41, and gene expression of HLA-B27 gene in ankylosing spondylitis patients and healthy control group. Read more about this study
- Who is it for?
- Ages 16 to 80 yearsHealthy volunteers can take part
- Conditions the study is for
- Ankylosing Spondylitis
- How many people
- 84 participants
- Where
- No sites listed yet
- Study dates
- 1 Mar 2026to 1 Mar 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 16 to 80 years
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: Participants will be recruited from the outpatient clinics of Rheumatology and Rehabilitation Department, Sohag University Hospitals.
Who may be able to join
- patients who are diagnosed clinically as ankylosing spondylitis (both active or stable), of either sex , who met the Assessment of Spondyloarthritis International Society (ASAS) criteria for axial spondyloarthritis.
Who cannot join
- Patients with any autoimmune disorder, chronic illnesses as diabetes mellitus, acute and chronic infectious diseases, malignancy.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Evaluation of the Relation Between Serum Interleukins 17, 38, 41, and HLA-B27 Gene Expression in Ankylosing Spondylitis Patients
The goal of this observational study is to measure the serum level of cytokines IL-17, IL-38,IL-41, and gene expression of HLA-B27 gene in ankylosing spondylitis patients and healthy control group.
The main question it aims to answer is:
Does the disease activity, severity, serum level of cytokines (IL-17, IL-38, and IL-41) are affected by the HLA-b27 gene positivity?
Researchers will compare the serum level of cytokines IL-17, IL-38,IL-41, and gene expression of HLA-B27 gene in ankylosing spondylitis patients and healthy control group to see if there significant differences in serum levels of interleukins 17, 38, 41 in AS patients and healthy control group.
.
Read the detailed description
Ankylosing spondylitis (AS) that is known as radiographic SpA (r-axSpA), is a type of axial spondyloarthritis, characterized by the dual pathology of inflammatory bone erosion and aberrant new bone formation. It is characterized by chronic inflammation affecting the sacroiliac joints and spine, leading over time to structural changes such as syndesmophyte formation and spinal ankylosis, with consequent impairment in function and quality of life. As an autoimmune disease, it may also affect several organs, including the eyes, intestines, heart, and lungs .
The global prevalence of AS ranges from 0.3 % to 1.4 %, with a strong predilection for young adult males, in whom mobility and quality of life are often severely impaired. Reports indicate that the global incidence of AS ranges from 0.07 to 0.32%, with a male prevalence 2-3 times higher than that of females .
The etiopathogenesis of spondylo-arthritis is still not fully understood but it has been described as involving several mechanisms of action that synergistically initiate and maintain a pro-inflammatory state, leading to disease onset . Numerous disciplines, including genetics, environment, gut microbiota, and hormones, have previously been studied in relation to the etiology of AS .
Genetic predisposition - particularly carriage of the Human Leukocyte Antigen B27 (HLA-B27) allele - is closely linked to AS susceptibility and underlies several immunopathogenic hallmarks of the disease. There is a growing interest in HLA-B27-based effects, particularly in HLA-B27(+) patients who have AS, although the diagnostic and prognostic functions of HLA-B27 in AS are still being contested. Patients with HLA-B27 positivity have a considerably younger age at onset, a greater number of cases of uveitis, and a higher frequency of involvement of peripheral joints compared to patients with HLA-B27 negative.
The development of inflammatory arthritis is dependent upon the presence of an unbalanced cytokine network. Several interleukins and chemokines, particularly those with pro-inflammatory effects such as tumor necrosis factor (TNF)-α, interleukin (IL)-17A and C-X-C motif chemokine ligand 10 (CXCL10), are involved in mediating inflammation and consequent tissue damage.
IL-17 is a pro-inflammatory cytokine that contributes to the pathogenesis of several inflammatory diseases. The IL-17 family consists of six structurally related cytokines (IL-17A, IL-17B, IL-17C, IL-17D, IL-17E, and IL-17F) . It is a key cytokine which promotes neutrophil recruitment and amplifies Th17 responses. Its serum concentration is also associated with inflammatory activity and response to IL-17 inhibitors.
IL-38 is a recently discovered member of the IL-1 family with anti-inflammatory functions. Functionally, IL-38 is broadly described as a cytokine with anti-inflammatory properties. Pro-inflammatory effects have also been identified and this may depend on IL-38 concentration. Increasing evidence indicates that IL-38 is a vital cytokine in the pathogenesis of several inflammatory autoimmune diseases, such as rheumatoid arthritis (RA), psoriatic arthritis. In AS, although systemic levels of IL-38 have not been determined, an association of IL38 gene polymorphism with AS risk has been proposed.
Metrnl, also referred to as Meteorin-like, Meteorin-b, Subfatin, Cometin, and IL-41, is a novel secretory protein involved in inflammation, immunology, and metabolic regulation that is abundant in organs related to metabolism and barrier tissues. Recent research suggested that Metrnl is involved in bone growth, development, remodeling, and related diseases. The roles of Metrnl in bone formation and resorption remain unclear, so further research is required to establish a clearer link between IL-41 and spinal inflammation in AS patients, which will contribute to understand pathogenesis of AS, and provides a way for the development of practical diagnostic tools and potentially more effective treatments.
The study is a case control study, will be done at Department of Medical Microbiology and Immunology in collaboration with Department of Rheumatology and Rehabilitation, Sohag University Hospitals. The practical part will be done in the Central Research Laboratory, Faculty of Medicine, Sohag University.
-The study will include 84 participants recruited from the outpatient clinics of Rheumatology and Rehabilitation Department, Sohag University Hospitals.
The participants will be divided as follows:
Group 1: 42 patients diagnosed with ankylosing spondylitis who met the 2009 Assessment of Spondyloarthritis International Society (ASAS) classification criteria for axSpA. Disease activity in AS was assessed using the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI).
Patients were stratified into two groups based on BASDAI scores: AS-Stable group (BASDAI ≤ 4) and AS-Active group (BASDAI > 4) Group 2: control group of 42 Age- and sex-matched healthy volunteers who do not suffer from inflammatory or autoimmune diseases belonging to same geographic region.
Aim of the Study:
- To measure the serum level of cytokines IL-17, IL-38, and IL-41 in ankylosing spondylitis patients (active and stable AS, including patients receiving TNF inhibitors and those not treated by TNF inhibitors) and healthy controls.
- To measure the gene expression of HLA-b27 gene by qRT-PCR in AS patients and controls.
Methods of the study:
- Full medical history taking (age, gender, degree of back pain using VAS, morning stiffness duration, and extraarticular manifestations (e.g., uveitis, and psoriasis), family history of AS or any autoimmune diseases, onset, duration of disease, associated diseases, medications, etc). The full patient information page data and consent forms will be completed under the direction of a rheumatologist.
- Clinical examination with special concern about peripheral, and axial joint examination.
- Evaluation of AS disease activity by Bath AS disease activity (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS), functional status by Bath ankylosing spondylitis functional index (BASFI).
- Comprehensive blood counts (CBC), erythrocyte sedimentation rates (ESR), and C-reactive protein (CRP) .
- The involvement of the sacroiliac joints will be assessed using the New York criteria.
- Sacroiliac joints resonance imaging as X rays and MRI.
- Specimen Collection: Five milliliters of fresh peripheral venous blood will be drawn of study participants and will be placed in tubes containing ethylene-diamine-tetra acetic acid (EDTA).
- Measuring the serum level of cytokines (IL-17, IL-38, IL-41) will be determined using a commercially available solid-phase enzyme immunoassay kit (ELISA).
- Measurement of gene expression of HLA-b27 gene in peripheral blood mononuclear cells by qRT-PCR.
Ethical consideration:
-Informed written consent will be obtained from the study group.
- Conditions
- Ankylosing Spondylitis
- Keywords
- Interleukin 17, Interleukin 38, Interleukin 41, HLA- B27 gene
- Medical subject headings
- Spondylitis, Ankylosing
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Cases | Patients with Ankylosing spondylitis | |
| Healthy Controls | Participants Without Ankylosing spondylitis |
What is being measured
The primary outcome is the main question the study is designed to answer.
collection of blood samples from paticipants
Measured: from March 2026 to August 2026
measurement of serum level of Interleukin 17 in participants
Measured: From September 2026 to October 2026
Measurement of serum level of Interleukin 38 in participants
Measured: from September 2026 to October 2026
measurement of serum level of Interleukin 41 in participants
Measured: from September 2026 to October 2026
measurement of gene expression of HLA- B27 gene in participants
Measured: from October 2026 to December 2026
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Feb 2026
- Study start1 Mar 2026 (estimated)
- Primary completion30 Dec 2026 (estimated)
- Study completion1 Mar 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Ankylosing SpondylitisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Enrolment
- 84 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Sohag University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Alaa Ezat Ahmed, Sohag University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07396194
- Sponsor's protocol ID
- Soh-Med-26-1-2MD
- Acronym
- Interleukins
- Status last verified
- Jan 2026
- First submitted
- 1 Feb 2026
- Last updated
- 9 Feb 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: 1. to avoid the reuse of data for unfair commercial purposes 2. to avoid the reuse of data for purposes that had not been approved by participants
Study at a glance
From the registry record, last updated by the sponsor on 9 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of the Relation Between Serum Interleukins 17, 38, 41, and HLA-B27 Gene Expression in Ankylosing Spondylitis Patients
- ClinicalTrials.gov ID
- NCT07396194
- Acronym / sponsor ID
- Interleukins / Soh-Med-26-1-2MD
- Conditions
- Ankylosing Spondylitis
- Keywords
- Interleukin 17, Interleukin 38, Interleukin 41, HLA- B27 gene
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 84 participants (estimated)
- Lead sponsor
- Sohag UniversityUniversity, hospital or other
- Study start
- 1 Mar 2026 (estimated)
- Primary completion
- 30 Dec 2026 (estimated)
- Study completion
- 1 Mar 2027 (estimated)
- First posted
- 9 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this observational study is to measure the serum level of cytokines IL-17, IL-38,IL-41, and gene expression of HLA-B27 gene in ankylosing spondylitis patients and healthy control group.
The main question it aims to answer is:
Does the disease activity, severity, serum level of cytokines (IL-17, IL-38, and IL-41) are affected by the HLA-b27 gene positivity?
Researchers will compare the serum level of cytokines IL-17, IL-38,IL-41, and gene expression of HLA-B27 gene in ankylosing spondylitis patients and healthy control group to see if there significant differences in serum levels of interleukins 17, 38, 41 in AS patients and healthy control group.
.
Detailed description
Ankylosing spondylitis (AS) that is known as radiographic SpA (r-axSpA), is a type of axial spondyloarthritis, characterized by the dual pathology of inflammatory bone erosion and aberrant new bone formation. It is characterized by chronic inflammation affecting the sacroiliac joints and spine, leading over time to structural changes such as syndesmophyte formation and spinal ankylosis, with consequent impairment in function and quality of life. As an autoimmune disease, it may also affect several organs, including the eyes, intestines, heart, and lungs .
The global prevalence of AS ranges from 0.3 % to 1.4 %, with a strong predilection for young adult males, in whom mobility and quality of life are often severely impaired. Reports indicate that the global incidence of AS ranges from 0.07 to 0.32%, with a male prevalence 2-3 times higher than that of females .
The etiopathogenesis of spondylo-arthritis is still not fully understood but it has been described as involving several mechanisms of action that synergistically initiate and maintain a pro-inflammatory state, leading to disease onset . Numerous disciplines, including genetics, environment, gut microbiota, and hormones, have previously been studied in relation to the etiology of AS .
Genetic predisposition - particularly carriage of the Human Leukocyte Antigen B27 (HLA-B27) allele - is closely linked to AS susceptibility and underlies several immunopathogenic hallmarks of the disease. There is a growing interest in HLA-B27-based effects, particularly in HLA-B27(+) patients who have AS, although the diagnostic and prognostic functions of HLA-B27 in AS are still being contested. Patients with HLA-B27 positivity have a considerably younger age at onset, a greater number of cases of uveitis, and a higher frequency of involvement of peripheral joints compared to patients with HLA-B27 negative.
The development of inflammatory arthritis is dependent upon the presence of an unbalanced cytokine network. Several interleukins and chemokines, particularly those with pro-inflammatory effects such as tumor necrosis factor (TNF)-α, interleukin (IL)-17A and C-X-C motif chemokine ligand 10 (CXCL10), are involved in mediating inflammation and consequent tissue damage.
IL-17 is a pro-inflammatory cytokine that contributes to the pathogenesis of several inflammatory diseases. The IL-17 family consists of six structurally related cytokines (IL-17A, IL-17B, IL-17C, IL-17D, IL-17E, and IL-17F) . It is a key cytokine which promotes neutrophil recruitment and amplifies Th17 responses. Its serum concentration is also associated with inflammatory activity and response to IL-17 inhibitors.
IL-38 is a recently discovered member of the IL-1 family with anti-inflammatory functions. Functionally, IL-38 is broadly described as a cytokine with anti-inflammatory properties. Pro-inflammatory effects have also been identified and this may depend on IL-38 concentration. Increasing evidence indicates that IL-38 is a vital cytokine in the pathogenesis of several inflammatory autoimmune diseases, such as rheumatoid arthritis (RA), psoriatic arthritis. In AS, although systemic levels of IL-38 have not been determined, an association of IL38 gene polymorphism with AS risk has been proposed.
Metrnl, also referred to as Meteorin-like, Meteorin-b, Subfatin, Cometin, and IL-41, is a novel secretory protein involved in inflammation, immunology, and metabolic regulation that is abundant in organs related to metabolism and barrier tissues. Recent research suggested that Metrnl is involved in bone growth, development, remodeling, and related diseases. The roles of Metrnl in bone formation and resorption remain unclear, so further research is required to establish a clearer link between IL-41 and spinal inflammation in AS patients, which will contribute to understand pathogenesis of AS, and provides a way for the development of practical diagnostic tools and potentially more effective treatments.
The study is a case control study, will be done at Department of Medical Microbiology and Immunology in collaboration with Department of Rheumatology and Rehabilitation, Sohag University Hospitals. The practical part will be done in the Central Research Laboratory, Faculty of Medicine, Sohag University.
-The study will include 84 participants recruited from the outpatient clinics of Rheumatology and Rehabilitation Department, Sohag University Hospitals.
The participants will be divided as follows:
Group 1: 42 patients diagnosed with ankylosing spondylitis who met the 2009 Assessment of Spondyloarthritis International Society (ASAS) classification criteria for axSpA. Disease activity in AS was assessed using the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI).
Patients were stratified into two groups based on BASDAI scores: AS-Stable group (BASDAI ≤ 4) and AS-Active group (BASDAI > 4) Group 2: control group of 42 Age- and sex-matched healthy volunteers who do not suffer from inflammatory or autoimmune diseases belonging to same geographic region.
Aim of the Study:
- To measure the serum level of cytokines IL-17, IL-38, and IL-41 in ankylosing spondylitis patients (active and stable AS, including patients receiving TNF inhibitors and those not treated by TNF inhibitors) and healthy controls.
- To measure the gene expression of HLA-b27 gene by qRT-PCR in AS patients and controls.
Methods of the study:
- Full medical history taking (age, gender, degree of back pain using VAS, morning stiffness duration, and extraarticular manifestations (e.g., uveitis, and psoriasis), family history of AS or any autoimmune diseases, onset, duration of disease, associated diseases, medications, etc). The full patient information page data and consent forms will be completed under the direction of a rheumatologist.
- Clinical examination with special concern about peripheral, and axial joint examination.
- Evaluation of AS disease activity by Bath AS disease activity (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS), functional status by Bath ankylosing spondylitis functional index (BASFI).
- Comprehensive blood counts (CBC), erythrocyte sedimentation rates (ESR), and C-reactive protein (CRP) .
- The involvement of the sacroiliac joints will be assessed using the New York criteria.
- Sacroiliac joints resonance imaging as X rays and MRI.
- Specimen Collection: Five milliliters of fresh peripheral venous blood will be drawn of study participants and will be placed in tubes containing ethylene-diamine-tetra acetic acid (EDTA).
- Measuring the serum level of cytokines (IL-17, IL-38, IL-41) will be determined using a commercially available solid-phase enzyme immunoassay kit (ELISA).
- Measurement of gene expression of HLA-b27 gene in peripheral blood mononuclear cells by qRT-PCR.
Ethical consideration:
-Informed written consent will be obtained from the study group.
Study design
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Cases | – | –Patients with Ankylosing spondylitis |
| Healthy Controls | – | –Participants Without Ankylosing spondylitis |
Who may qualify
- Ages
- 16 to 80 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Participants will be recruited from the outpatient clinics of Rheumatology and Rehabilitation Department, Sohag University Hospitals.
Key inclusion criteria (1 listed)
- patients who are diagnosed clinically as ankylosing spondylitis (both active or stable), of either sex , who met the Assessment of Spondyloarthritis International Society (ASAS) criteria for axial spondyloarthritis.
Key exclusion criteria (1 listed)
- Patients with any autoimmune disorder, chronic illnesses as diabetes mellitus, acute and chronic infectious diseases, malignancy.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
collection of blood samples from paticipants
Time frame: from March 2026 to August 2026
measurement of serum level of Interleukin 17 in participants
Time frame: From September 2026 to October 2026
Measurement of serum level of Interleukin 38 in participants
Time frame: from September 2026 to October 2026
measurement of serum level of Interleukin 41 in participants
Time frame: from September 2026 to October 2026
measurement of gene expression of HLA- B27 gene in participants
Time frame: from October 2026 to December 2026
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Feb 2026.
- Individual participant dataSharing planned: No. 1. to avoid the reuse of data for unfair commercial purposes 2. to avoid the reuse of data for purposes that had not been approved by participants
Related trials for Ankylosing Spondylitis
Not yet recruitingObservational study
Pain Phenotyping of Rheumatic Diseases - An Observational Study
Rheumatic Diseases, Lupus Erythematosus, Systemic
Active, not recruitingObservational study
Frequency and Complications of Major Orthopedic Procedures in Medicare Beneficiaries
Rheumatoid Arthritis, Ankylosing Spondylitis
Not yet recruitingPhase 4
Ivarmacitinib With or Without Celecoxib for Ankylosing Spondylitis
Ankylosing Spondylitis (AS)
RecruitingPhase 3
An Open-label Study to Evaluate the Pharmacokinetics and Safety of Bimekizumab in Pediatric Study Participants With Active Juvenile Idiopathic Arthritis Subtypes Enthesitis-related Arthritis (Including Juvenile-onset Ankylosing Spondylitis) and Juvenile Psoriatic Arthritis
Enthesitis-related Arthritis, Juvenile Psoriatic Arthritis
RecruitingPhase 2
A Clinical Study of Tulisokibart (MK-7240) to Treat Radiographic Axial Spondyloarthritis (MK-7240-013)
Radiographic Axial Spondyloarthritis
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
An observational study of Ankylosing Spondylitis, run by Sohag University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 9 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Alaa Ezzat Ahmed, Assisstant lecturer (00201008908404, alaa.ezzat@med.sohag.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
collection of blood samples from paticipants (time frame: from March 2026 to August 2026). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Feb 2026.