# Proof-of-concept study evaluating humoral primary immunodeficiencies via CJ:KREC ratio and serum BAFF level

**Authors:** Elisa Ochfeld, Amer Khojah, Wilfredo Marin, Gabrielle Morgan, Lauren M. Pachman

PMC · DOI: 10.1038/s41598-024-64942-4 · 2024-06-21

## TL;DR

This study explores new ways to measure B cell activity in patients with humoral primary immunodeficiencies using CJ:KREC ratios and serum BAFF levels.

## Contribution

The study introduces CJ:KREC ratio and serum BAFF as potential biomarkers for assessing humoral primary immunodeficiencies.

## Key findings

- CVID patients showed elevated CJ:KREC ratios compared to controls, though not statistically significant.
- CVID patients with lymphoproliferative features had significantly higher serum BAFF levels.
- BAFF levels were higher in antibody deficiency syndromes compared to controls.

## Abstract

Humoral primary immunodeficiencies are the most prevalent form of primary immunodeficiency (PID). Currently, there is no convenient method to quantify newly formed B cells. The aim of this proof-of-concept study was to quantitate the ratio of coding joints (CJs) to Kappa-deleting recombination excision circles (KRECs) and serum B cell activating factor (BAFF) in patients with humoral primary immunodeficiency and assess if they correlate with disease severity. This IRB-approved study was conducted at one academic children’s hospital. Patients with humoral PIDs and healthy controls were included. CJ and KREC levels were measured via qPCR. Serum BAFF levels were measured using Mesoscale. 16 patients with humoral PID and 5 healthy controls were included. The mean CJ:KREC ratio in the CVID, antibody deficiency syndromes, and controls groups, respectively were 13.04 ± 9.5, 5.25 ± 4.1, and 4.38 ± 2.5 (p = 0.059). The mean serum BAFF levels in CVID, antibody deficiency syndromes and controls were 216.3 ± 290 pg/mL, 107.9 ± 94 pg/mL and 50.9 ± 12 pg/mL, respectively (p = 0.271). When the CVID patients were subdivided into CVID with or without lymphoproliferative features, the BAFF level was substantially higher in the CVID with lymphoproliferation cohort (mean 372.4 ± 361 pg/mL, p = 0.031). Elevated CJ:KREC ratio was observed in CVID, although statistical significance was not achieved, likely due to the small sample size. Serum BAFF levels were significantly higher in CVID patients with lymphoproliferative features. We speculate that the CJ:KREC ratio and serum BAFF levels can be utilized in patients with humoral PID, once more extensive studies confirm this exploratory investigation.

## Linked entities

- **Proteins:** TNFSF13B (TNF superfamily member 13b)
- **Diseases:** antibody deficiency syndromes (MONDO:0003778)

## Full-text entities

- **Genes:** TNFSF13B (TNF superfamily member 13b) [NCBI Gene 10673] {aka BAFF, BLYS, CD257, TALL-1, TALL1, THANK}
- **Diseases:** lymphoproliferative (MESH:D008232), CVID (MESH:D017074), antibody deficiency syndromes (MESH:D007153), PID (MESH:D000081207)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11192915/full.md

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Source: https://tomesphere.com/paper/PMC11192915