Detection of chronic lymphocytic leukemia subpopulations in peripheral blood by phage ligands of tumor immunoglobulin B cell receptors

The B cell receptor (BCR) is an immunoglobulin (Ig) expressed on the membrane surface of mature B cells [1]. The IgBCR has two heavy and two light chains, each one made by a constant and a variable region. The variable sequences of the IgBCR are generated during B-cell differentiation through somatic recombination, so called VDJ recombination, and somatic hypermutation [2]. Once assembled on the B-cell surface, the IgBCR recognizes a specific antigen through its binding to the variable regions. This event triggers the B-cell immune response against the antigen. Since the variable regions are B cell specific, the sequence of IgBCR allows the identification of single B-cell clones [3]. In B-lymphoproliferative disorders, the IgBCR plays a key role in the development, proliferation, and survival of tumor B cells [4], by an antigen-driven process that triggers a molecular cascade of events that lead to transcriptional activation of proliferative and antiapoptotic genes [5–7]. Chronic lymphocytic leukemia (CLL) is a Bproliferative disorder characterized by a clonal expansion and accumulation of neoplastic CD19/CD5/CD23/ CD20-positive B-lymphocytes in blood, bone marrow, and other tissues [8]. Several studies support the hypothesis that a common pool of environmental antigens or self-antigens drives the selection of tumor B cells through the persistent triggering of IgBCR [9, 10]. Consistently, the sequence analysis of VDJ rearrangement of tumor IgBCRs revealed a high level of homology in more than 30% of CLL patients, defined as stereotyped IgBCR, with the prevalence of VH1, VH3, and VH4 families [11, 12]. CLL are defined as mutated (M-CLL) or unmutated (U-CLL) depending on the mutational rate of the IgBCR variable regions, being more or less than 2% respect to the germline, respectively [11, 12]. U-CLL cells expressing the VH1-69 rearrangement usually have an inducible IgBCR and show an aggressive behavior [11, 12]. In this regard, it would be useful to develop new molecular tools for rapid detection of aggressive CLL clones in peripheral blood. We previously used phage display for identifying peptide ligands of B-lymphoma, multiple myeloma, and CLL IgBCRs [3, 13–15]. In CLL patients, we documented the co-existence of different CLL clones in a single patient as detected by phage-expressed peptide ligands of the tumor IgBCRs [3, 15]. In this study, we used the phage display for identifying a peptide sequence that was commonly recognized by VH1-69 U-CLL clones of two CLL patients. These patients, named CLL#1 and CLL#5, were randomly referred to the Hematology Unit—University Federico II of Naples and initially diagnosed as CLL Binet stage A. At month 8, CLL#1 worsen to Binet stage C and returned to Binet stage A after 6 months of These authors contributed equally: Selena Mimmi, Domenico Maisano


To the Editor:
The B cell receptor (BCR) is an immunoglobulin (Ig) expressed on the membrane surface of mature B cells [1]. The IgBCR has two heavy and two light chains, each one made by a constant and a variable region. The variable sequences of the IgBCR are generated during B-cell differentiation through somatic recombination, so called VDJ recombination, and somatic hypermutation [2]. Once assembled on the B-cell surface, the IgBCR recognizes a specific antigen through its binding to the variable regions. This event triggers the B-cell immune response against the antigen. Since the variable regions are B cell specific, the sequence of IgBCR allows the identification of single B-cell clones [3]. In B-lymphoproliferative disorders, the IgBCR plays a key role in the development, proliferation, and survival of tumor B cells [4], by an antigen-driven process that triggers a molecular cascade of events that lead to transcriptional activation of proliferative and antiapoptotic genes [5][6][7].
Chronic lymphocytic leukemia (CLL) is a Bproliferative disorder characterized by a clonal expansion and accumulation of neoplastic CD19/CD5/CD23/ CD20-positive B-lymphocytes in blood, bone marrow, and other tissues [8]. Several studies support the hypothesis that a common pool of environmental antigens or self-antigens drives the selection of tumor B cells through the persistent triggering of IgBCR [9,10]. Consistently, the sequence analysis of VDJ rearrangement of tumor IgBCRs revealed a high level of homology in more than 30% of CLL patients, defined as stereotyped IgBCR, with the prevalence of VH1, VH3, and VH4 families [11,12]. CLL are defined as mutated (M-CLL) or unmutated (U-CLL) depending on the mutational rate of the IgBCR variable regions, being more or less than 2% respect to the germline, respectively [11,12]. U-CLL cells expressing the VH1-69 rearrangement usually have an inducible IgBCR and show an aggressive behavior [11,12]. In this regard, it would be useful to develop new molecular tools for rapid detection of aggressive CLL clones in peripheral blood.
We previously used phage display for identifying peptide ligands of B-lymphoma, multiple myeloma, and CLL IgBCRs [3,[13][14][15]. In CLL patients, we documented the co-existence of different CLL clones in a single patient as detected by phage-expressed peptide ligands of the tumor IgBCRs [3,15]. In this study, we used the phage display for identifying a peptide sequence that was commonly recognized by VH1-69 U-CLL clones of two CLL patients. These patients, named CLL#1 and CLL#5, were randomly referred to the Hematology Unit-University Federico II of Naples and initially diagnosed as CLL Binet stage A. At month 8, CLL#1 worsen to Binet stage C and returned to Binet stage A after 6 months of therapy. CLL#5 was stably CLL Binet stage A for 2 years of observation. In the course of disease, we analysed four blood samples of patient CLL#1 (CLL#1 a-d) and three blood samples of patient CLL#5 (CLL#5 a-c). Clinical and laboratory data are reported in Supplementary Table  S1. Total RNA was extracted from purified B cells and reverse transcribed in cDNA followed by nested RT-PCR to amplify the heavy and light chains of the Ig variable regions, as previously described [3] (Supplementary Fig.  S1). The PCR-amplified products were appropriately digested and cloned in expression vectors for DNA sequencing. The Ig nucleotide sequences were analysed by the international ImMunoGeneTics information sys-tem® (IMGT® http://www.imgt.org) in order to find a match with the relative VH and VL families, according to the classification of the stereotyped IgBCRs. In both CLL patients, we observed the co-existence of variable VH nucleotide sequences, both U-CLL and M-CLL, with a unique VL nucleotide sequence at each time of collection (Table 1) (GenBank accession numbers MT334403 to MT334414).
Among the total CLL populations, an unmutated VH1-69 CLL subpopulation persisted in the patient CLL#1 (VH1-69/D3-16*01/J6*02) and patient CLL#5 (VH1-69/ D7-27*01/J3*02) all time of observation, ranging between 30 and 80% of total CLL population. Other CLL clones were either mutated or unmutated, appearing and disappearing over time at a lower percentage (Table 1). In the patient CLL#1, the VH1-69 clone peaked at 80% at passage to Binet stage C and dropped to 30% after therapy with the remission of disease (Table 1). This evidence indicated that the VH1-69 U-CLL clone had an aggressive behavior as, differently from the other CLL clones, it persisted elevated during the time of observation.
We reasoned that a specific ligand could be a potential tool to discriminate and monitor the VH1-69 U-CLL subpopulation in peripheral blood. To this end, we produced the recombinant CLL IgBCRs, as previously described [3] (Supplementary Fig. S2). The purified VH1-69 U-CLL Ig of patient CLL#5 was used as bait to screen an M13 phage-displayed random peptide library (RPL) [3,16]. The workflow of phage selection is shown in Supplementary Fig. S3. Twenty-five phage colonies were selected and subject to DNA sequencing to determine the amino acid sequence required for the binding to the VH1-69 U-CLL Ig. Three amino acid sequences were identified at different frequencies: p1 (48% phages), p2 (35% phages), and p3 (17% phages) (Fig. 1a). By ELISA, the phage p1 showed higher affinity binding to VH1-69 U-CLL Ig of patient CLL#5 compared with phages p2 and p3 (Fig. 1b) (Supplementary Fig. S4). Further, the phage p1 did not bind the other three CLL clones of patient CLL#5, while phage p2 and p3 did (Fig. 1b). We then analysed the binding of the three phages to the CLL Igs of patient CLL#1. The phage p1 bound only the VH1-69 U-CLL Ig of CLL#1 with high affinity (Fig. 1b). Differently, the phages p2 and p3 did not bind VH1-69 U-CLL Ig of CLL#1 and showed a weak binding to other Igs of patient CLL#1 (Fig. 1b). These results indicated that the phage p1 exclusively bound the VH1-69 U-CLL IgBCR of both patients CLL#1 and CLL#5 (Fig. 1b).
Being the VH1-69 rearrangement of IgBCR often associated with poor prognosis of CLL [12], we considered the possibility to detect the VH1-69 U-CLL population in peripheral blood using phage p1 as specific ligand. To this end, we analysed the immunophenotype and phage binding profile of B cells collected from patient CLL#5 at month 1. Consistently with clinical data (Supplementary Table S1), B cells were 99.5% CD5positive and expressed the IgM isotype and the lambda light chain (Fig. 1c-e). As control, the phage wild type did not show any binding (Fig. 1f). The phage p1 detected 73.5% of CD5-positive cells, and the phage p2 and phage p3 detected 86.0% and 81.6%, respectively ( Fig. 1g-i). These results were consistent with the occurrence of 75% VH1-69 U-CLL clones in the patient CLL#5 as detected by VDJ sequence (Table 1) and the specific binding of phage p1 to the relative VH1-69 U-CLL IgBCR (Fig. 1b). The progressive dilution of B-CLL cells with healthy PBMCs caused a parallel decrease of phage p1-positivity, confirming the specific binding of the phage p1 to the target tumor clones (Fig. 1l-p). Thus, the phage p1 revealed to be a specific probe for detecting the VH1-69 U-CLL population within a mix of blood cells.
CLL harbors different tumor clones in a single CLL patient, which can be identified by the IgBCR structure. Sequencing the tumor IgBCRs determines the variability of tumor clones but is not useful for flow cytometry of tumor clones in real time. To date, the diagnosis of disease is based on the evaluation of total number of CD5-positive cells associated with the stage of lymphoid tissues infiltration. In this context, it would be relevant to have sensitive molecular tools for monitoring the different tumor clones based on IgBCR recognition. This would be possible by developing new reagents for flow cytometry in order to detect and eventually isolate the most aggressive CLL subpopulations for molecular characterization. Our study opens to the possibility to monitor CLL clones in the peripheral blood of patients by using phage ligands as specific probes of CLL subpopulations. In perspective, the validation of this experimental approach on a large number of patients could provide a new method of clusterization of CLL clones based on their epitopic reactivity.   Publisher's note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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