ClinicalTrials.gg
Enrolling by invitationNCT02422875Updated Oct 1, 2026

Comparative Autoantibody and Immunologic Cell Marker Study

An observational study in Autoimmune Diseases, Lupus Erythematosus, Systemic and Communicable Diseases, sponsored by Emory University. Enrolling by invitation at 3 sites in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-01.

Primary conditionLupus Erythematosus, SystemicRegistry: Autoimmune DiseasesReclassifiedWhy we changed it
Registry
Autoimmune Diseases — the first condition term the registry derived for this study.
ClinicalTrials.gg
Lupus Erythematosus, Systemic
Why
  1. The study's listed conditions name Lupus Erythematosus, Systemic, a narrower term within Autoimmune Diseases.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Emory University · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
2,500
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to compare immune phenotype, function, and specificity of B lymphocytes from different developmental stages in autoimmune patients to B cells from infectious disease patients and healthy controls.

Read the detailed description

Systemic lupus erythematosus (SLE) is an autoimmune disease (in autoimmune illness, the immune system in the body attacks it's own cells, leading to illness). It is not completely understood how this disease develops in the body. In a normal person, there is a tolerance of antigens (substances that make antibodies, which protect the body from disease-causing agents). Research in mice suggests that defects in certain types of cells can make the body lose this tolerance, therefore recognizing antigens made in the body as foreign, and mounting an immune response to the "self", thus causing autoimmune disease. In this study, the researchers will look at these potentially defective cells in people with SLE and other autoimmune diseases and compare them to cells in healthy participants, as well as looking at the blood of first-degree relatives of people with autoimmune disease.

The study involves blood draws and bone marrow aspirates. Participants may be asked to donate 2/3 to about 9 tablespoons of blood. The volume of blood needed will depend on the experiment being done as different numbers of cells are necessary to run different experiments. Study participants may return for additional blood draws will not donate blood more than twice a week, and will not have more than 16 tablespoons of blood drawn in a one-month period. Participants donating bone marrow will have about 3 ½ tablespoons of bone marrow obtained, which will be drawn with a large needle from the bone located in the back of the hip. Bone marrow participants may be asked to donate up to 7 tablespoons of blood as well, in order to correlate the blood with the bone marrow sample and the populations of cells residing in each. Participants donating bone marrow may donate more than once, but must wait a minimum of 8 weeks between donations.

02

Conditions studied

  • Autoimmune Diseases
  • Lupus Erythematosus, Systemic
  • Communicable Diseases

Keywords

  • Sjögren's Syndrome
  • Scleroderma
  • Myositis
  • Juvenile Idiopathic Arthritis
  • Rheumatoid Arthritis
  • Inflammatory Arthritis
  • Undifferentiated Connective Tissue Disease
  • Idiopathic thrombocytopenic purpura
  • Graft vs Host Disease
  • Autoimmune Lymphoproliferative Syndrome
  • Immunoglobulin G4 (IgG4)-related disease
  • Hepatitis C
  • Epstein Barr Virus (infectious mononucleosis - EBV)
  • Sepsis
  • Guillain-Barre syndrome
  • Mycoplasma pneumoniae
  • Human Immunodeficiency Virus
03

In context

Lupus Erythematosus, Systemic Reclassified

1,207 studies on the registry are indexed under Lupus Erythematosus, Systemic; 405 are open to participants now.

This study's planned enrollment of 2,500 is above the median of 151 across 280 observational studies indexed under Lupus Erythematosus, Systemic.

Browse Lupus Erythematosus, Systemic studies →

Lead sponsor

Emory University is the lead sponsor of 1,405 studies on the registry; 225 are open to participants now.

Of its 237 completed or terminated interventional studies of FDA-regulated products, 178 (75%) have results posted.

Compared within Lupus Erythematosus, Systemic, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Autoimmune Diseases. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

  • Subjects with certain autoimmune conditions or if subjects have brothers, sisters, mother, father, or children with an autoimmune condition
  • Subjects with certain infectious diseases
  • Subjects who are without an autoimmune condition or infectious disease
  • Subjects who have received or will receive a vaccination as part of their regular standard of care from one of their healthcare providers

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Signed written by the subject or, if the subject is unable to provide informed consent, the subject's legal representative may provide consent.
  • Subjects can be of either gender
  • Subjects with diseases, and Systemic Lupus Erythematosus (SLE) patients will fulfill the American College of Rheumatology Classification criteria for SLE to be determined by their treating physician but may have incomplete criteria (\<4 items). SLE patients are not restricted by treatment or by disease activity as determined by Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) or Systemic Lupus Activity Measure (SLAM) score

    1. Subjects with acute exacerbations of their disease, including hospitalized patients
    2. First-degree relatives of subjects with active disease
  • Subjects who have received or will receive a vaccination may be enrolled for bone marrow aspirates before and/or after vaccination. Vaccination will have been done by the subject's healthcare provider or through another outside source.
  • Subjects may have a screening blood draw performed in cases where a certain subset of cells or antibody titer is desired. This may be followed by additional blood draws and/or bone marrow aspiration after the ideal candidates have been identified.
  • Subjects who have been diagnosed with or another infectious disease
  • Subjects taking biologic and/or immune modulatory agents in diseases such as cancer, allergy, and pulmonary diseases will be enrolled.
  • Healthy controls must be free of acute or chronic disease at the time of bone marrow donation. Healthy controls that are first-degree relatives of subjects with active disease will be enrolled as well.

Exclusion criteria

Exclusion Criteria:

  • Poor venous access
  • Subjects who have had side effects to local anesthetics such as lidocaine and who are on blood thinners such as warfarin
  • Normal controls must be free of acute or chronic diseases or medications that may affect the assay (as determined by the investigator).
  • For subjects donating bone marrow, insufficient access to the iliac crest such that the periosteum and bone is hindered based on normal aspiration procedures.
  • Pregnant or lactating women may not donate bone marrow.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
2,500 participants (estimated)
Target follow-up
3 Days
Patient registry
Yes
Biospecimen retention
Samples with dna

Groups and cohorts

  • Healthy Controls

    Subjects are healthy persons without any autoimmune conditions or infectious diseases

  • Autoimmune Disease

    Subjects diagnosed with autoimmune disease including but not limited to: Systemic Lupus Erythematosus (SLE), Sjögren's Syndrome (SS), Scleroderma, Myositis, Juvenile Idiopathic Arthritis (JIA), Rheumatoid Arthritis (RA), inflammatory arthritis, undifferentiated connective tissue disease, idiopathic thrombocytopenic purpura (ITP), Graft vs Host Disease (GVHD), Autoimmune Lymphoproliferative Syndrome (ALPS) and IgG4-related disease

  • Infectious Disease

    Subjects diagnosed with an infectious disease including but not limited to: Hepatitis C, Epstein Barr Virus (infectious mononucleosis - EBV), Sepsis, Guillain-Barre syndrome (GBS), Mycoplasma pneumoniae or Human Immunodeficiency Virus (HIV)

  • Autoimmune - Family

    Subjects have a brother, sister, mother, father, or child with an autoimmune disease

  • Vaccination

    Subjects have received or will receive a vaccination as part of regular standard of care from their healthcare provider or other outside source

06

What researchers measure

Primary outcomes

  1. Distribution of autoreactive B cells within bone marrow

    B cells will be analyzed using flow cytometry.

    Time frame: Baseline

07

Study locations

3 sites
08

Timeline

1 registry update since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Aug 2012, a primary completion of May 2028 and a completion of May 2028. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 17, 2015
First posted
Apr 21, 2015
Start
Aug 2012
Primary completionEst.
May 2028
CompletionEst.
May 2028
Last update
Oct 1, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Minor edits
Nothing that changes what the study is or who can join. Edited: identifiers, verification date and oversight details
1 update, last Oct 1, 2026
Show all 1 update
  1. Oct 1, 2026
    Minor edits only
    + 3 other changes: identifiers, verification date and oversight details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT02422875
Lead sponsor
Emory University
Responsible party
Ignacio Sanz (Professor, Emory University) — Principal investigator
First posted
Apr 21, 2015
Start date
Aug 2012
Primary completion
May 2028 (estimated)
Completion
May 2028 (estimated)
Last update
Oct 1, 2026

Study contacts

Ignatio Sanz, MD
principal investigator · Emory University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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