Expanded clinical and experimental use of SOX11 - using a monoclonal antibody
© Nordström et al.; licensee BioMed Central Ltd. 2012
Received: 13 February 2012
Accepted: 15 May 2012
Published: 27 June 2012
The transcription factor SOX11 is of diagnostic and prognostic importance in mantle cell lymphoma (MCL) and epithelial ovarian cancer (EOC), respectively. Thus, there is an unmet clinical and experimental need for SOX11-targeting assays with low background, high specificity and robust performance in multiple applications, including immunohistochemistry (IHC-P) and flow cytometry, which until now has been lacking.
We have developed SOX11-C1, a monoclonal mouse antibody targeting SOX11, and successfully evaluated its performance in western blots (WB), IHC-P, fluorescence microscopy and flow cytometry.
We confirm the importance of SOX11 as a diagnostic antigen in MCL as 100% of tissue micro array (TMA) cases show bright nuclear staining, using the SOX11-C1 antibody in IHC-P. We also show that previous reports of weak SOX11 immunostaining in a fraction of hairy cell leukemias (HCL) are not confirmed using SOX11-C1, which is consistent with the lack of transcription. Thus, high sensitivity and improved specificity are demonstrated using the monoclonal SOX11-C1 antibody. Furthermore, we show for the first time that flow cytometry can be used to separate SOX11 positive and negative cell lines and primary tumors. Of note, SOX11-C1 shows no nonspecific binding to primary B or T cells in blood and thus, can be used for analysis of B and T cell lymphomas from complex clinical samples. Dilution experiments showed that low frequencies of malignant cells (~1%) are detectable above background using SOX11 as a discriminant antigen in flow cytometry.
The novel monoclonal SOX11-specific antibody offers high sensitivity and improved specificity in IHC-P based detection of MCL and its expanded use in flow cytometry analysis of blood and tissue samples may allow a convenient approach to early diagnosis and follow-up of MCL patients.
KeywordsSOX11 Flow cytometry Immunohistochemistry Transcription factor B cell lymphoma diagnostics
The transcription factor SOX11 has recently been identified as a diagnostic, prognostic and/or functional antigen in a variety of cancers including mantle cell lymphoma (MCL) [1–6], epithelial ovarian cancer (EOC) [7, 8] and gliomas . This transcription factor is a member of the SOX protein family, which is characterized by a conserved high mobility DNA binding domain (HMG) . Of major clinical interest, the expression of SOX11 in non-malignant tissues is limited to immature neurons  and embryonic [11–13] and neural development [14, 15].
This tissue-restricted expression facilitates specific identification of malignant cells in clinical samples and has enabled the use of this target for specific diagnosis of MCL, as shown in a number of studies [1–6]. SOX11 expression has also been reported in a fraction of other T and B-cell lymphomas, including B- and T-cell lymphoblastic lymphomas and a subset of Burkitts lymphoma [3, 16], but the most common B-cell lymphomas lack SOX11 expression. Thus, using SOX11 as a diagnostic marker for MCL avoids misclassification of morphologically similar CD5+ marginal zone lymphomas (MZL) or CD23- chronic lymphocytic leukemia (CLL). In addition, several studies suggest that SOX11 is a prognostic indicator in MCL, although it remains to be confirmed whether negative cases identify a rare indolent subtype [4, 17] or, conversely, patients with a shorter survival . Furthermore, in EOC, SOX11 has prognostic significance and identifies a subgroup of patients with improved recurrence-free survival  and may also identify an histological subtype of EOC . Finally, we have recently published data, demonstrating a growth regulatory role for SOX11 in in-vitro models of MCL  and EOC , which was further confirmed using xenotransplants in mice . Together these data suggest a key growth regulatory role of SOX11 in these neoplasms and emphasize the need for functional antibodies for experimental use in various technologies, including imaging and flow cytometry applications.
Polyclonal antibodies targeting SOX11 have been widely used in immunohistochemistry on paraffin sections (IHC-P) [2, 3, 5, 7, 8, 16]. However, batch to batch variations of commercially available reagents have prevented routine clinical use where standardized protocols are a prerequisite. Furthermore, there is increasing desire for expanded use of flow cytometry in immunoprofiling of tumors. This technology has already been used for several decades to confirm B cell clonality and characterize the phenotype of cellular constituents in aspirates and sections of lymphoproliferative disorders . Although rarely used as the sole tool for diagnosis, studies have shown that flow cytometry is both a sensitive and specific method to identify, and in many cases, classify B cell lymphomas . In contrast to IHC, flow cytometry enables quantitative measurements at the single cell level and provides the ability to analyze and quantify the co-expression of proteins in defined subpopulations, in a manner superior to immunohistochemistry . However, reagents targeting SOX11 in flow cytometry have until now been lacking.
In this study, we demonstrate that the monoclonal SOX11-C1 antibody enables improved use of SOX11 as a diagnostic antigen in MCL. This antibody provides high sensitivity and improved specificity in IHC, which has enabled reclassification of previously positive HCL cases. Furthermore, the SOX11-C1 antibody allowed detection of SOX11 by flow cytometry and immunofluorescence microscopy. To assess the potential to identify rare MCL cells in blood through flow cytometry analysis, dilution experiments were performed, which permitted detection of <1% MCL cells, using SOX11 as the single discriminate antigen. In summary, the novel SOX11-C1 antibody fulfills a clinical need for increased specificity in IHC-P and extends its diagnostic utility to flow cytometry analysis.
Generation and characterization of monoclonal SOX11 antibodies
Mouse monoclonal antibodies raised against a C-terminal part of SOX11 were generated using hybridoma technology . SOX11 reactivity and lack of reactivity to the purification tag (hexahistidyl albumin binding tag, His-ABP) was assessed in ELISA and 19 clones were isolated and subcloned. Antibody isotyping revealed a high percentage of clones encoding the IgM heavy chain (68%) but clones encoding IgG could also be identified (26% IgG1 and 5% IgG2a). Concentration of selected antibodies (n = 5, all IgG1) were assessed and ranged between 1.6 and 4.6mg/ml.
Immunohistochemistry-based validation of SOX11-C1
Patient characteristics and SOX11 staining
Age range (mean)
SOX11-C1 staining (P/T)1
Flow cytometry based validation of SOX11-C1antibody
Cell line characteristics and SOX11 status
Mantle cell lymphoma
Mantle cell lymphoma
Mantle cell lymphoma
Mantle cell lymphoma
Mantle cell lymphoma
Mantle cell lymphoma
Acute B-lymphoblastic leukemia/lymphoma Acute T-lymphoblastic leukemia/lymphoma
Differentiated ovarian clear cell carcinoma
Primary malignant adenocarcinoma
Immunohistochemistry and flow cytometry-based analysis of SOX11 in tumor xenografts
Immunofluorescence microscopy-based analysis of SOX11
Flow cytometry analysis of SOX11 in primary lymphocytes and malignant cells
Furthermore, to assess the sensitivity of SOX11 as a discriminant antigen in flow cytometry-based assays, leukemic MCL samples were mixed with normal PBMC (ratio MCL:PBMC; 1:0; 1:1, 1:10, 1:100, 1:000 and 0:1) and analyzed (Figure 6d). Analysis of non-MCL populations showed that the SOX11-C1 antibody stained ≤0.3% of the control cells. The percentage of positive cells decreased from 65% (pure MCL) down to 48% (1:1), 15.4% (1:10), 1.6% (1:100) and 0.3% (1:1000). The data is representative of two independent MCL donors. Using SOX11 as a single discriminate antigen, malignant cells were readily detected above background down to a dilution of 1:100, i.e. a population of cells containing 1.6% MCL cells. Of note, identification of tumor cells in flow cytometry normally requires the use of multiple markers and advanced gating strategies, emphasizes the strength of SOX11 as a discriminate antigen.
SOX11 has recently been shown to have important diagnostic and prognostic value in MCL, EOC and glioma [1–5, 7, 8, 24]. As the expression of SOX11 is restricted to immature neurons in the healthy adult , specific detection of SOX11 positive malignant cells is feasible using IHC-P in most tissues. However, previous reports, where a polyclonal antibody was used, show cytoplasmic and nuclear staining of SOX11 in FL [1, 3, 5, 16] and HCL [5, 16], respectively, despite lack of SOX11 transcription .
Considerable efforts are needed to standardize antibodies for clinical use in IHC-P. Reproducible detection of a specific antigen is dependent on multiple parameters, including type and concentration of fixative, incubation time, antigen retrieval, antibody concentration and detection system [25–27]. This is exemplified by the limited availability of antibodies targeting SOX11 in IHC-P; only two out of more than thirty commercially available antibodies targeting SOX11 can be successfully used in IHC-P [1, 2, 5, 7, 8, 16, 28]. Furthermore, batch to batch variation of polyclonal antibodies is a concern, and has limited the routine clinical use of SOX11.
To overcome these limitations, we developed a monoclonal antibody raised against a C-terminal peptide of SOX11, p-SOX11c-term, which has no homology to the closely related protein SOX4 . This feature minimizes the possibility of cross-reactivity to SOX4 in B and T lymphocytes, which would compromise analysis of SOX11 in complex tissues. Monoclonal antibodies, such as the SOX11-C1 antibody, are consequently of great importance since they offer single epitope specificity and no batch to batch variation. Additionally, a hybridoma clone in murine or hamster cell lines enables large-scale production at low cost, as recently reviewed by Yamada .
We show, using the monoclonal SOX11-C1 antibody, that 100% of the MCL cases (TMA) tested presented nuclear staining of SOX11, suggesting a disease-defining property. This is in accordance with recent reports, in which SOX11 also was shown to identify rare cases of cyclin D1-negative MCLs with either typical  or blastoid  morphology. However, the rare occurrence of SOX11 negative cases, was confirmed in a single MCL case, defined by 11;14 translocation and immunophenotyping. Future investigations using large, well-defined patient series will provide reliable statistics on the infrequent occurrence of SOX11-negative MCLs. Of interest, several cases of bone marrow biopsies of HCL with previously weak nuclear staining  where reclassified as negative, in accordance with their lack of mRNA. Thus, this novel monoclonal SOX11-specific antibody shows high sensitivity and improved specificity in IHC-P, emphasizing its value in diagnosis and follow-up. However, future studies are needed to determine the frequency of SOX11 positive cases among primary Burkitt’s and T- and B lymphoblastic lymphomas.
As previously discussed, flow cytometry has emerged as an important clinical tool in the diagnosis and follow-up of patients after treatment. Also for intracellular antigens such as cyclin D1, successful detection of tumor cells has been shown in >90% of cases with blood involvement . However, to enable assessment of cyclin D1 overexpression in patient samples, highly standardized procedures are required . To determine whether the SOX11-C1 antibody allow intracellular detection of SOX11 in flow cytometry, we performed a proof-of-principle assay and analyzed well-defined lymphoma and EOC cell lines. In agreement with mRNA expression and previous WB data , SOX11 positive cell lines where distinguished from negative ones in all cases, which implies high specificity and sensitivity of flow cytometry analysis of SOX11. Of note, SOX11 was detected in KM3, an acute B lymphoblastic leukemia cell line, and support previous findings of SOX11 positive B lymphoblastic lymphomas using IHC-P . Also in a more complex setting, using a single cell suspension derived from a tumor established by intravenous injection of Z138 MCL cells into NSG mice, SOX11-C1 was able to distinguish SOX11-positive from negative samples.
To evaluate the potential clinical use of flow cytometry in patients with disseminated SOX11-positive disease, dilution experiments where performed. We demonstrate that malignant cells, comprising as little as 1% of the total lymphocyte population are detectable, using SOX11 as the sole discriminant antigen. Future attempts to replicate these findings in patients with various degree of disseminated disease and in combination with immunophenotyping would be of great interest. In combination, the simplicity of the flow cytometry protocol and the disease-defining property of the SOX11 antigen suggest its future use in both routine diagnostics and for detection of circulating tumor cells during patient follow-up. For potential assessment of minimal residual disease, careful comparison with IGH-PCR needs to be performed as, flow cytometry has shown to be inferior to IGH-PCR at follow-up after treatment . This difference in sensitivity may be partly related to the clearance of B cells upon rituximab (anti-CD20) treatment, thereby increasing the relative sensitivity of IGH-PCR based detection.
There is an unmet clinical and experimental need for specific and sensitive analysis of SOX11 in relation to SOX11-positive tumors, including MCL and EOC. The novel SOX11 monoclonal antibody, SOX11-C1, offers improved functionality, such as (i) immunofluorescence-based investigations (ii) improved specificity in IHC-P, enabling more sensitive and specific diagnosis and (iii) flow cytometry-based detection, which is potentially feasible in aspirates from MCL and for detection of circulating tumor cells.
Generation of monoclonal antibodies targeting SOX11
SOX11-specific peptide used for immunization
Subcultivation of cell lines and assessment of SOX11 mRNA expression
A number of lymphoma/leukemia and EOC cell lines, including Z138, GRANTA-519, JEKO-1, SP53, REC-1, JVM-2, RL, DOHH-2, BJAB, KM3, MOLT-4, ES-2, OVCAR-3, and TOV-112D, were purchased from ATCC or DSMZ (or when not available, received as kind donations, see acknowledgement). Lymphoid cell lines were cultured in RPMI-1640 (Thermo Scientific HyClone, Logan, UT, USA) supplemented with 10% fetal bovine serum (Invitrogen, San Diego, CA, USA) and 2 nM L-glutamine (Invitrogen). EOC cell lines where cultured in either McCoy’s (Thermo Scientific HyClone) + 10% FBS and 2 mM L-glutamine (ES-2), DMEM high glucose (Thermo Scientific HyClone) + 10% FBS and 2 mM L-glutamine (TOV-112D) or RPMI-1640 + 20% FBS + 2 mM L-glutamine + 0.01 mg/ml insulin (Sigma-Aldrich) (OVCAR-3). All cell lines were kept under standard conditions (5% CO2, 37°C). The relative quantity (RQ) of SOX11 mRNA in these cell lines was measured with real time-quantitative PCR (RT-PCR), as previously described . The RQ is calculated as 2-(ΔΔCT(SOX11-GAPDH)) and cell lines with a ΔCT (SOX11+RT, SOX11-RT) > |2| were defined as SOX11 positive. Error bars have been calculated using the standard error value with 95% confidence interval.
Evaluation of the SOX11-C1 antibody in Western blot using B cell lymphoma cell lines
Protein lysate (30 μg) obtained from B cell lymphoma cell lines were run on a NuPAGE 10% Bis-Tris gel (Invitrogen). Proteins were blotted onto a PVDF membrane with the iBlot® Dry Blotting System (Invitrogen) and the membrane was blocked in 5% milk/PBS. SOX11 expression was assessed using SOX11-C1 at a final concentration of 1 μg/ml in 5% milk/PBS. A primary antibody targeting GAPDH was used as loading control and a HRP labeled rabbit anti-mouse antibody (Dako, Glostrup, Denmark) was used for detection. Labeled proteins were visualized using SuperSignal West Femto Max Sensitivity Substrate (Pierce Biotechnology, Rockford, IL, USA), and images retrieved using a CCD camera (FluorSMax, Biorad). Proteins were quantified, using the Volume Rect Tool (Quantity One, Biorad), and the relative volume of the background was set to 1.
Flow cytometry analysis of SOX11 in B cell lymphoma and EOC cell lines
Lymphoma/leukemia and EOC cell lines were fixed in 4% paraformaldehyde (PFA) (Thermo Scientific) for 10 minutes. The cells were subsequently permeabilized in PBS supplemented with 5% FCS and 0.5% Triton X-100 (Sigma Chemical Co., St Louis, USA). SOX11 was stained using SOX11-C1 antibody at 1 μg/ml for 16 h. Primary antibody and unstained control cells were detected using goat anti-mouse-APC (BD Bioscience, San Jose, CA, USA). All samples were analyzed on FACS Canto II (BD Bioscience) and FCS Express 4 Flow Research Edition (De Novo Software, Los Angeles, CA USA) was used for data analysis.
Sequencing of immunoglobulin genes coding for the SOX11-C1 antibody
The immunoglobulin genes coding for SOX11-C1 were sequenced in both heavy and light chain variable regions (VH, VL) according to standard procedures (Absea Biotechnology Ltd, Beijing, China).
Immunohistochemistry analysis using SOX11-C1 antibody
SOX11-C1 monoclonal antibody was tested on a tissue microarray (TMA) consisting of fifteen MCL, fourteen CLL, fifteen follicular lymphomas (FL), two Burkitt’s lymphomas and thirteen tonsil sections. Additionally, whole sections of one MCL, two Burkitt’s lymphomas, seven HCL, two B-lymphoblastic lymphomas, four T-lymphoblastic lymphomas and five normal bone marrows were tested. Tumors developing after intravenous injection of Z138 in NOD SCID gamma (NSG) mice were prepared, as previously described . Bone marrow biopsies from HCL were fixed in 10% formalin and decalcified until softened in a solution of ethanol, nitric acid and chromium trioxide at room temperature, while bone marrows obtained from healthy donors or B-lymphoblastic lymphomas were decalcified in a solution of EDTA at 37°C. All samples were routinely processed and embedded in paraffin for tissue conservation. Antigen retrieval was performed using the PT-LINK system (Dako) at pH 9. Staining was performed using SOX11-C1 (1-2ug/ml). For detection, Envision + System HRP (Dako) was used on a DAKO autostainer Plus (Dako). Staining of a single HCL case using a polyclonal reagents targeting SOX11, was performed as previously described [3, 16].
Affinity estimations using competitive ELISA
The affinity of the SOX11-C1 antibody to its antigen was estimated, using a competitive setup in ELISA. Briefly, a high binding microtiter plate was coated with p-SOX11c-term (10 ng/well). After blocking, a fixed concentration of SOX11-C1 (0.1 μg/ml) was pre-incubated with the antigen, p-SOX11c-term, at an optimized concentration range (0–100 nM) for 1 hour. The amount of unbound antibodies in solution was measured with ELISA. The dissociation constant (KD) was estimated to equal the antigen concentration at 50% signal inhibition.
Image analysis of SOX11 using fluorescence microscopy
Slides for image analysis were prepared by (i) immobilization of lymphoma cells (40,000 cells/slide) onto a glass slide, using a cytospin (Shandon, Pittsburgh, USA) or (ii) cultivation of EOC cells in eight-well chamber slides (Nalge Nunc International, Rochester, NY, USA). Cells were fixed in 4% PFA for 10 min followed by permeabilization (PBS supplemented with 5% FCS and 0.5% Triton X-100, (Sigma Chemical Co)). Cells were stained with SOX11-C1 antibody (1 μg/ml, overnight) followed by a goat anti-mouse IgG-ALEXA 568 reagent (Invitrogen). The nuclei were counterstained with DAPI (Invitrogen/Dynal) and mounted with Pro Long Gold anti-fade medium (Invitrogen). Images were captured (exposure time; DAPI 40 ms, TX RED 2 s) using a fluorescence microscope (Nikon Eclipse 80i, Nikon Instrument Inc. NY, USA) equipped with Nis Element BR (Nikon).
Flow cytometry analysis of SOX11 in NSG mice-derived tumors
Tumors were established in female NSG mice (The Jackson Laboratory, Sacramento, California, USA, (bred at Lund University for multiple generations)) by intravenous injection of Z138 cells (0.5 × 106 cells) carrying SOX11-specific (SOX11-knocked) or scrambled (control) shRNA sequences. Animals were sacrificed when presenting symptoms of disease, as previously described . All animal experimentation was strictly performed in accordance with the regulations of the Lund University Ethics Committee (Dnr M229-09).
Single cell suspensions from tumors developing in the ovaries were prepared. Cells were stained in two separate tubes, i.e., (i) extracellular with HLA-DR-APC (BD Biosciences) or (ii) stained with SOX11-C1 after fixation and permeabilization, as described above. FSC and SSC gating strategy was based on HLA-DR positive cells as a marker for human B cells. The same gating strategy was used to assess SOX11 expression in the complex mixture of cells.
Flow cytometry analysis of SOX11 in primary B cell lymphomas
Peripheral blood mononuclear cells (PBMC) from two leukemic MCL (L-MCL) patients and two non-malignant blood donors were isolated by Ficoll (VWR) gradient centrifugation, according to standard procedures. Furthermore, single-cell suspensions from three MCL, two FL, and two non-malignant tonsil biopsies were prepared by dissection of tissue, with resultant diffusion of malignant cells into the media (RPMI-1640). Malignant cells (L-MCL) were mixed with PBMC at the following ratios; 1:0 1:1, 1:10, 1:100, 1:1000 and 0:1. For each sample, 500,000 cells were stained with SOX11-C1 antibody as described above but with the following modifications: after addition of goat anti-mouse-APC the samples were blocked with mouse IgG (Jackson ImmunoResearch Laboratories Inc., West Grove, PA, USA) for 30 minutes followed by staining with CD3-PE (Invitrogen) and CD20-FITC (Dako).
Chronic lymphocytic lymphoma/leukemia
Enzyme linked immunosorbent assay
Hairy cell leukemia
Immunohistorychemistry using paraffin embedded tissue
Mantle cell lymphoma
Immunoglobulin heavy chain
NOD SCID gamma
Peripheral blood mononuclear cells
Variable heavy chain
Tissue micro array
Variable light chain
Whole tissue section.
Kristina Lövgren is acknowledged for all her help and support with IHC stainings. Dr. Gabriella Honeth, Lund University, Dr Martin Dyer, Leicester University and Prof R Brown, Imperial College, London are all gratefully acknowledged for providing cell lines for the study. The study was supported by the Lund Institute of Technology (LTH), Cancerfonden (09/0390), CREATE Health, a strategic Center for Translational Cancer Research (http://www.createhealth.lth.se), Stiftelsen Olle Engkvist Byggmästare, Crafoord foundation and BioCARE – a strategic program for Cancer Research at Lund and Gothenburg Universities.
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