- Open Access
Circulating monocytes and tumor-associated macrophages express recombined immunoglobulins in glioblastoma patients
Clinical and Translational Medicinevolume 8, Article number: 18 (2019)
Glioblastoma is the most common and malignant brain tumor in adults. Glioblastoma is usually fatal 12–15 months after diagnosis and the current possibilities in therapy are mostly only palliative. Therefore, new forms of diagnosis and therapy are urgently needed. Since tumor-associated macrophages are key players in tumor progression and survival there is large potential in investigating their immunological characteristics in glioblastoma patients. Recent evidence shows the expression of variable immunoglobulins and TCRαβ in subpopulations of monocytes, in vitro polarized macrophages and macrophages in the tumor microenvironment. We set out to investigate the immunoglobulin sequences of circulating monocytes and tumor-associated macrophages from glioblastoma patients to evaluate their potential as novel diagnostic or therapeutic targets.
We routinely find consistent expression of immunoglobulins in tumor-associated macrophages (TAM) and circulating monocytes from all glioblastoma patients analyzed in this study. However, the immunoglobulin repertoires of circulating monocytes and TAM are generally more restricted compared to B cells. Furthermore, the immunoglobulin expression in the macrophage populations negatively correlates with the tumor volume. Interestingly, the comparison of somatic mutations, V-chain usage, CDR3-length and the distribution of used heavy chain genes on the locus of chromosome 14 of the immunoglobulins from myeloid to B cells revealed virtually no differences.
The investigation of the immunoglobulin repertoires from TAM and circulating monocytes in glioblastoma-patients revealed a negative correlation to the tumor volume, which could not be detected in the immunoglobulin repertoires of the patients’ B lymphocytes. Furthermore, the immunoglobulin repertoires of monocytes were more diverse than the repertoires of the macrophages in the tumor microenvironment from the same patients suggesting a tumor-specific immune response which could be advantageous for the use as diagnostic or therapeutic target.
Macrophages are omnipresent versatile immune cells with myeloid origin. Due to their function as phagocytes they are assigned to the innate immune system where they play a key role in chronic inflammation [1, 2].
Traditionally, the expression of combinatorial immune receptors represented by immunoglobulins (Ig) and T cell receptors (TCR) is thought to be an exclusive competence of lymphoid effector cells like B and T cells [2, 3]. However, in the past decade several publications provided evidence for the recombination of variable immune receptors in cells not belonging to the lymphoid lineage [4, 5]. The initial observations by Puellmann et al. in 2006 demonstrated the expression of variable αβ T cell receptors in a subpopulation of neutrophil granulocytes [6,7,8]. Ensuing studies showed the recombination of TCR αβ/γδ in monocytes and macrophages [9, 10] as well as TCR γδ in eosinophils . Interestingly, recent studies present the induction of TCRβ expression in neutrophils and macrophages during malaria infection [12, 13]. Furthermore, an implication of these TCR based myeloid variable immune receptors in several chronic diseases like autoimmune disease , chronic periodontitis , tuberculosis  and atherosclerosis  was shown. Additionally, our laboratory demonstrated the recombination of variable TCRαβ by macrophages in the tumor microenvironment . Importantly, most recent studies from our laboratory and others provided evidence for the expression of the second variable immune receptor based on immunoglobulin heavy and light chain genes by myeloid immune effector cells [18,19,20].
Traditionally, macrophages are divided into M1 and M2 categories. In the tumor milieu, M1 macrophages are typically tumor-suppressive and M2 macrophages serve an anti-inflammatory, tumor-supportive role . The tumor-associated macrophages (TAM) play a key role in the host’s immune response to the tumor. Typically, TAM are attributed to promote tumor growth and progression in two different ways, directly by stimulating tumor cell proliferation and indirectly by creating an immunosuppressive microenvironment [22,23,24,25,26]. Moreover their infiltration is associated with a poor clinical outcome in cancer patients [27, 28]. But despite all these findings, the exact role of tumor-associated macrophages is still controversial.
Glioblastoma multiforme (GBM) is the most common malignant tumor of the central nervous system in adults with a global incidence of 0.59–3.69/100,000 . It is associated with poor prognosis and a median patient survival of 12–15 months from diagnosis [30, 31]. The long-term survival for glioblastoma patients, which is considered to be more than 3 years from diagnosis, is only at around 3–5% [32, 33]. Since GBM is rapidly fatal, therapy includes surgical resection to the extent feasible, adjuvant radiotherapy and temozolomide chemotherapy and is mostly only palliative [30, 34, 35].
Future prospects in the treatment of glioblastoma tend to immunotherapies or targeting of the tumor microenvironment. As the exact immunological features of TAM in glioblastoma is still unknown, we investigated the immunoglobulin repertoires of monocytes/macrophages in the tumor tissue and peripheral blood of 17 glioblastoma patients and compared them to the immunoglobulin repertoires of corresponding B cells. Detailed analyses of the immunoglobulin sequences are needed as these myeloid immunoglobulins might represent novel biological targets, since immunoglobulin variants are discussed as potential biomarkers and therapeutics in cancer .
In summary, the goal of this study is to determine whether patients with glioblastoma have a specific repertoire of myeloid antibodies, if there are differences in the immunoglobulin repertoires of circulating monocytes and tumor-associated macrophages from glioblastoma patients and if the myeloid antibodies can be a useful tool as therapeutic or diagnostic target in glioblastoma.
Materials and methods
All 17 patients included in the study suffered from glioblastoma, which was assigned to WHO grade IV. After prior written consent, tumor tissue and peripheral blood for study purposes were obtained during surgery. The average age of the patients was 58 years with an age range from 43 to 74 years. An overview of the patient’s characteristics is listed in Additional file 1: Table S1.
Cell isolation from tumor tissue/blood and purity control
Both the tissue and the blood samples were processed immediately after collection in the operating room. The fresh tumor tissue was manually divided into small pieces with a sterile single-use scalpel and enzymatically digested with a solution of DNase I (500 U/ml) and collagenase IV (190 U/ml) in RPMI at 37 °C and 5% CO2 on a rotator for at least 90 min. Finally, the cell suspension was filtered and washed with PBS.
The blood sample was diluted 1:1 with PBS (Sigma Aldrich) and separated by density gradient centrifugation using Ficoll-Paque PLUS solution (GE Healthcare Life Sciences). The white layer of PBMCs was transferred to a fresh tube and washed with PBS. If necessary, one or two erythrocyte lysis steps followed. Subsequently, the cell suspensions from tumor and blood sample were subjected to CD14 and CD19 Magnetic Cell Sorting (MACS, Miltenyi Biotec) to isolate monocytes/macrophages as well as B cells. The purified cell fractions were resuspended in 1 ml of TRIzol LS Reagent, respectively (Thermo Fisher). The purity of the isolated cell fractions was either tested by flow cytometry or the absence of B and T cells was demonstrated by using a highly sensitive PCR protocol.
Repertoire-PCRs of immunoglobulins
For the analysis of gene expression, RNA was isolated according to the TRIzol LS Reagent manual by Thermo Fisher. cDNA synthesis was carried out using equal amounts of RNA to get comparable results in the following PCR. For every isolated cell fraction a quality control PCR was conducted using primers for GAPDH, CD2, CD14, CD19, CD68 and CD163. Repertoire-PCRs for the desired immunoglobulins were performed for all cell fractions which passed the quality control. Depending on the studied antibody class, one reverse primer in the constant region of the specific immunoglobulin sequence and four to seven different consensus forward primers in the variable regions were used. In total, four antibody classes (IgM, IgG, Igκ, Igλ) were investigated. The sequences of the primers used in this study can be provided upon request.
Cloning and Sanger sequencing
For the generation of the immunoglobulin sequences, the PCR products were cloned into competent E. coli (Top10) by using the TOPO TA Cloning Kit for Sequencing (Thermo Fisher) according to the manufacturer’s protocol. The generated plasmids were purified out of liquid cultures using the GeneJET Plasmid Miniprep Kit (Thermo Fisher). Sequencing PCR was performed using the BigDye Terminator v1.1 Cycle Sequencing Kit (Thermo Fisher). The amplified sequencing-PCR-products were purified with the NucleoSEQ kit from Macherey–Nagel and then used for Sanger sequencing on an ABI Prism 310.
For the analyses of the sequencing results the databases igBLAST and VBASE2 were used. All alignments, mutation analyses and the construction of an own database were done using CLC Genomics Workbench by Qiagen.
CD14 immunostaining and HE staining of glioblastoma tissue was performed using standard protocols in the department of neuropathology of the university hospital Heidelberg. Analysis of the staining was conducted on an Olympus microscope IX70 with the camera “Progres Gryphax” by Jenoptik.
Cytokine release assay
The cytokine levels in the patient’s serum were analyzed using the Milliplex MAP Human Cytokine/Chemokine Magnetic Bead Panel (Merck Millipore). The patient samples and seven healthy controls were collected during the study and stored at − 20 °C until the last patient was included. The assay was performed according the manufacturer’s protocol with the standards and quality controls in duplicates and all samples in triplicates. The plate was analyzed using the Milliplex Analyzer (Merck Millipore).
Quantitative volumetry of the tumors
All brain tumor volume measurements were performed using the iPlan Cranial Software 3.0.5 (Brainlab AG).
The student’s t-test was used to compare the significance of repertoire diversity, mutation rate and cytokine release between the different cell groups. *p > 0.05 and **p < 0.001 was considered statistically significant. The Shannon diversity index is a mathematical tool to estimate variability of the immunoglobulin repertoires. It is expected that monoclonal and oligoclonal samples have low values, and highly diverse samples result in higher values [37, 38].
High purity of the monocyte/macrophage cell preparations
Recent evidence revealed the expression of immunoglobulins from macrophage subpopulations in the tumor microenvironment . In this proof-of-principle study, different tumor entities were tested for the presence of the immunoglobulin expressing TAM subpopulation including one patient with glioblastoma. Here, we systematically investigated immunoglobulin repertoires of TAM from 17 glioblastoma patients (Additional file 1: Table S1) and compared them to the circulating monocytes of the same patients. To address this, we first established a protocol for the reproducible isolation of CD14+ cells from venous blood and tumor tissue. The purity of the isolated monocyte/macrophage populations was tested by flow cytometry. As these experiments showed a purity of > 99% the quality of the isolation method was confirmed (Fig. 1a). Using a highly sensitive quality control PCR protocol the isolated cell fractions routinely showed no characteristic gene expression of B and T cell markers (Fig. 1b, Additional file 1: Figure S1). Furthermore, the presence of the myeloid markers CD14, CD68 and CD163 confirmed the isolated cells to be monocytes/macrophages (Fig. 1b). Consequently, the highly pure isolated cell fractions were used for further analysis of the immunoglobulin expression. Of note, expression of the secreted and membrane form of IgG could be identified in the monocyte/macrophage cell preparations from healthy individuals and glioblastoma patients (Additional file 1: Figure S2A).
Higher immunoglobulin diversity in circulating monocytes than in the tumor-associated macrophages
We analyzed the CDR3 heavy and light chain Ig repertoires expressed by TAM and monocytes obtained from 15 patients with glioblastoma during surgery. In order to do this, the IgM, IgG, Igκ and Igλ repertoire diversities were determined by cloning and Sanger sequencing of the expressed Ig CDR3 variants. Peripheral blood B cells and B cells isolated form the tumor from three representative glioblastoma patients (GBM003; GBM004; GBM008) were co-analyzed as reference. In total, 1293 immunoglobulin sequences coding for 456 unique CDR3 sequences were included in this study.
Hence, analysis of the immunoglobulin expression revealed diverse immunoglobulin heavy and light chain repertoires of monocytes and tumor-associated macrophages in all glioblastoma patients. Interestingly, the immunoglobulin diversity between monocytes and B cells from the blood and macrophages isolated from the corresponding tumor sample of the same patient differed strongly (Additional file 1: Figure S3A). In all patients, the diversity of the expressed immunoglobulins in the circulating monocytes was much higher than in the corresponding tumor-associated macrophages (Fig. 2, Additional file 1: Figure S4). Furthermore, the immunoglobulin expression level of circulating monocytes was usually higher than in TAM (Additional file 1: Figure S2B). These results were also reflected by the Shannon Diversity Indices 0.95 for monocytes and 0.42 for TAM (Additional file 1: Figure S3B). The size of the immunoglobulin repertoires from the circulating monocytes as well as the tumor-associated macrophages of different patients was individual specific. Large variances from eighteen different immunoglobulin heavy chain clonotypes in the circulating monocytes and only two different clonotypes in the tumor-associated macrophages from one patient were found. A similar phenomenon could be identified in the immunoglobulin light chain repertoires (Fig. 2, Additional file 1: Figure S4).
Inter- and intra-individual overlaps of immunoglobulin CDR3 variants
Most of the immunoglobulin CDR3 nucleotide sequences from TAM and monocytes (97.8% of all immunoglobulin heavy and light chain CDR3 variants) were found in only one subject. However, five immunoglobulin heavy chain CDR3-regions were found that were expressed in more than one patient (Table 1). In the B cell preparations from three representative GBM patients no CDR3 heavy chain sequences were shared between the different patients. However, we found two immunoglobulin heavy chain sequences in the B cell preparations shared between blood and tumor of the same patient (Additional file 1: Table S2). In the monocytic cells, we found seven immunoglobulin heavy chain sequences in blood and tumor of the same patient. The immunoglobulin light chain sequences showed slightly more overlapping sequences in monocytes and TAM (ten CDR3 variants) as well as in the B cells (four CDR3 variants) (Table 1 and Additional file 1: Table S2). Summarizing, most of the myeloid immunoglobulin heavy and light chain sequences are individual specific but show a higher percentage of shared CDR3 variants than the B lymphocytic cells.
Diversity of the immunoglobulin repertoire from the tumor-associated macrophage inversely correlates with the tumor volume
The diversity of the immunoglobulin repertoires in TAM and monocytes varied strongly between the individual patients. The patient characteristics (tumor stage, IDH mutation, ARTX mutation, etc.) of the glioblastoma patients included in our study were quite uniform (Additional file 1: Table S1). However, one characteristic distinction between the single patients is their unique tumor volume which ranged from 3 to 92 ml.
Surprisingly, the diversities of the expressed immunoglobulin repertoires in TAM and monocytes, respectively, decrease with increasing tumor volume (Fig. 3a–d). The decrease of diversity with increasing tumor volume was more pronounced in monocytes. The inverse correlation is indicated by correlation coefficients between − 0.603 and − 0.977. Especially the light chains show a strong significant correlation with p = 0.029 for TAM and p = 0.014 for monocytes (Fig. 3c, d). Importantly, the number of CD14+ cells isolated from the tumor and blood samples did not correlate with the tumor volume (Additional file 1: Figure S5), and histological analysis revealed an infiltration of a diverse number of CD14+ cells in tumors of different sizes (Additional file 1: Figure S6). Of note, other patient characteristics showed no correlation with the immunoglobulin CDR3 repertoire of monocytes and TAM (data not shown).
Contrasting to the immunoglobulin repertoire from macrophages, the immunoglobulin diversity from B cells showed no correlation with the tumor size (Fig. 3e).
Immunoglobulin repertoire features of the CDR3 sequences from myeloid cells and B cells
A detailed analysis of the myeloid and B cell immunoglobulin repertoires was performed to investigate if the differences in immunoglobulin repertoire size between the cell populations are based on sequence specificities. Therefore, reference alignment and structural analysis of the immunoglobulin sequences of TAM and B cells from three representative patients provided detailed sequence information, such as the exact V gene and J gene usage and CDR3 length. Analysis of the immunoglobulin heavy and light chain CDR3 lengths from TAM and B cells varied only slightly between TAM and B cells (Fig. 4a). As expected, the CDR3 sequences originating from B cells demonstrated Gaussian-type profiles. In contrast, the CDR3 length distribution in TAM showed a more oligoclonal profile in the three patients analyzed.
Additionally, the distribution of the sequenced VH- and JH-families was investigated. For this purpose, the expressed IgM and IgG heavy chains of all glioblastoma-patients were summarized, grouped into families and compared to the corresponding B cells (Fig. 4b). Most of the expressed VH-segments from tumor-associated macrophages and B cells (76% and 68%, respectively) belong to the VH3-family while the rest is equally distributed among the other five families. The most used JH-chains are JH4 with 53% in macrophages and 52% in B cells followed by JH5 (21% and 17%) and JH6 (15% and 14%), respectively. This is in accordance with previously published numbers for normal B cells .
Thus, based on this analysis, we found that the distributions of immunoglobulin VH- and JH-family genes were comparable between B cells and TAM. Of note, the three most expressed VH-genes in monocytes and TAM are 3-30-3*01 (64×), 3-21*01 (39×) and 3-33*01 (32×) whereas B cells expressed predominantly 3-33*01 (22×), 6-1*01 (13×) and 3-11*01 (12×).
Analysis of the chromosomal localization of VH-region genes
Next, to assess whether the restriction of the immunoglobulin repertoires in TAM had its origin in the localization of the VH region genes on the chromosome, VH region genes were mapped regarding to their chromosomal location for a comparative overview. The VH region genes of the Ig heavy chains are located at the telomeric end of chromosomal band 14q32.33.
The immunoglobulin repertoires of macrophages and B cells from three representative glioblastoma patients with a small, medium and large tumor were analyzed (GBM003, GBM004, GBM008; Fig. 4c). Here, VH region genes expressed by B cells were widely distributed over the entire locus with different levels of expression as expected. In contrast, the VH region genes expressed by TAM of the same patients were clustered in the center of the locus. However, the clustering was less pronounced when immunoglobulin VH region genes expressed by TAM and monocytes from all GBM patients analyzed in this study were taken into account (Additional file 1: Figure S7).
Similar mutation frequencies of immunoglobulin VH-Region genes expressed by tumor-associated macrophages and B cells
Functional antibodies are assembled by V-(d)-J gene rearrangement and then diversified by somatic hypermutation. The restricted immunoglobulin repertoire diversities in monocytes/macrophages compared to B cells prompted us to analyze the mutation frequencies of immunoglobulin VH-region genes in macrophages and B cells. Therefore, the number of somatic mutations in macrophages as well as in B cells was quantified to examine if a lower number of somatic mutations provided an explanation for the smaller repertoire sizes. Interestingly, comparing the mutation frequencies of immunoglobulin VH region genes from TAM and the corresponding circulating monocytes revealed a higher mutation frequency in TAM than in monocytes although they have a less diverse repertoire. This could be demonstrated for immunoglobulin heavy and light chain V region genes, respectively (Fig. 5a).
Of note, the overall number of mutations in the VH region genes of IgM and IgG from macrophages and B cells showed a similar distribution for both cell types (Fig. 5b). But in general, the number of somatic mutations in IgG sequences was significantly higher than in IgM sequences.
Thus, the differences in the immunoglobulin repertoire diversities between macrophages and B cells are not based on distinct abilities for somatic hypermutation.
Impaired immunocompetence of monocytic cells from GBM patients
GBM is described to be associated with systemic immune suppression . In this regard, the immune status of the GBM patients was evaluated on the basis of cytokine release in the patients serum, HLA-DR expression of myeloid cells and hematological cell counts. The immune status was analyzed to examine if the restricted immunoglobulin repertoires might be based on impaired immunocompetence of the myeloid cell compartment. To test the overall immune status of the GBM patients in this study, serum cytokine levels of the GBM patients were compared to healthy controls. A number of pro-inflammatory cytokines/chemokines including CCL2 (MCP-1), CCL22 (MDC), sCD40L, CXCL10 (IP-10), CXCL8 (IL-8), EGF and CCL3 (MIP-1α) were (in some cases significantly) decreased in GBM patients compared to healthy controls suggesting a lowered immune competence in GBM patients (Fig. 6, Additional file 1: Figure S8A). Most of these cytokines are primarily produced by monocytes/macrophages and may represent an impaired immune status of these myeloid cells. Interestingly, the anti-inflammatory cytokine IL-10 is increased in the glioblastoma patients which has already been reported in association with immunosuppression in glioblastoma , whereas TNFα serum levels were unaltered (Additional file 1: Figure S8B).
Hematological analyses in all patients revealed on average slightly elevated white blood cell counts with decreased lymphocyte, elevated neutrophil and normal monocyte cell counts (data not shown). These conditions have been previously described in glioblastoma patients .
HLA-DRA expression in monocytes has been described as a marker for immune competence. Especially in septic patients but also in the context of cancer, low HLA-DRA levels have been reported [40, 43]. A tendency to lower HLA-DRA expression in monocytic cells especially of TAM from GBM patients in this study compared to expression levels in monocytes from healthy individuals are demonstrated (Additional file 1: Figure S9). Consequently, several evidences for impaired immunocompetence of immune cells especially monocytes in the glioblastoma patients are detected and which are not based on decreased numbers of monocytes in the peripheral blood.
Glioblastoma multiforme is the most common brain tumor in adults that is characterized by a marked heterogeneity at the cellular and molecular level . In GBM, tumor-infiltrating microglia and peripheral macrophages are major immune cell populations within the tumor accounting for up to 30% of tumor mass in human GBMs . In a recent study, we presented the expression of recombined immunoglobulin heavy and light chains in tumor-associated macrophages isolated from various types of tumor tissue . In the present study, we were able to show, for the first time, the constitutive expression of immunoglobulin heavy and light chains in tumor-associated macrophages and circulating monocytes in a cohort of glioblastoma patients. Of note, the soluble and the transmembrane forms of immunoglobulins were demonstrated in monocytes and macrophages.
Importantly, highly diverse and individual-specific immunoglobulin heavy and light chain repertoires were detected in the circulating monocytes and in macrophages from tumor tissue of all 15 glioblastoma patients analyzed in this study. However, the immunoglobulin repertoire diversity in the myeloid cells was highly restricted compared to the B cells of three representative patients. This is in accordance with previous reports about restricted variable immunoglobulin and T cell receptor repertoire expression in myeloid cells [9, 17, 18, 20]. Of note, all sequences in this study were generated by cloning and Sanger sequencing of PCR products generated with consensus primers. A primer bias could be ruled out due to the significant differences of the expressed VH genes between the myeloid and B cell populations. Moreover, the number of somatic mutations within the immunoglobulin sequences, the chromosomal localization of the expressed VH-genes, the CDR3 length, and the use of VH and JH chain-family genes did not show significant differences between monocytes/macrophages and the B lymphocytic cells. This suggests a pathway of recombination of the individual immunoglobulin gene segments in the myeloid cells which is very similar or even identical to the mechanism used in B cells.
In addition to the lower immunoglobulin diversity in TAM and monocytes compared to B cells, we were able to demonstrate an inverse correlation of the immunoglobulin repertoires with the respective individual tumor size of the GBM patients. For the investigated light chains this inverse correlation was statistically significant (p = 0.029 and p = 0.014), while the significance level of 5% was missed for the heavy chains in both cases. In the future, by extending the patient population and using a high-throughput sequencing approach, however, statistical significance will probably be achieved. The inverse correlation was specific for the myeloid cell compartment and could not be detected in B cells. In the tumor microenvironment, infiltrating macrophages have been described as antitumor M1 as well as protumoral M2 phenotypes . These functional phenotypes are defined by differential expression of surface markers, secreted cytokines, and roles in immunoregulation . However, clinical and mouse model data correlate the accumulation of macrophages with protumoral activities [22,23,24,25]. Due to the negative dependence of antibody diversity and tumor size, an immunosuppressive effect of the tumor and its microenvironment on the immunoglobulin-expressing macrophages and monocytes might be conceivable. Larger tumors seem to have stronger suppressive effects on the immunoglobulin expression of myeloid cells than smaller tumors. Importantly, the suppressive effect seems to be more pronounced within the tumor than in the periphery. The observed lowered cytokine release and lowered HLA-DR expression of monocytic cells in the GBM patients are in line with this hypothesis. Impaired immunocompetence on the level of cytokine release and other features have been reported in several studies of glioblastoma [46, 47].
On the other hand, an alternative explanation for our results showing even more restricted immunoglobulin repertoires in the TAM compartment than in the circulating monocytes might be conceivable. Similar results were obtained in studies where variable immune receptors of tumor-infiltrating lymphocytes (TIL) were compared to circulating lymphocytes [48, 49]. These studies showed a clonal restriction due to oligoclonal expansion in the TIL compartment suggesting an adaptation to- or a modification by the tumor microenvironment. Mohme et al. conclude that TIL have undergone antigen-induced activation and should be able to mount a cytotoxic anti-tumor response . Correspondingly, due to the limited immunoglobulin diversity in TAM a tumor-specific selection of TAM leading to specific immunoglobulin expression could be reasonable. In line with this is the high frequency of somatic mutations in the variable regions which indicates that the tumor-infiltrating macrophages locally produce restricted immunoglobulin repertoires with evidence of antigen-driven maturation. It might therefore be possible that the immunoglobulins expressed by TAM are implicated in the anti-tumor immune response. Conceivably, the restricted antigen-specific immunoglobulin variants expressed by the monocytic lineage could be a useful as diagnostic or therapeutic target. Indicative for this is that a more detailed analysis of the macrophage immunoglobulin repertoires revealed that the expressed immunoglobulin CDR3 variants show intra-individual overlaps between the peripheral blood and tumor compartment, as well as inter-individual overlaps of the repertoires between several patients. Interestingly, in almost half the patients we find shared immunoglobulin CDR3 variants between circulating monocytes and tumor-associated macrophages isolated from the same patients suggesting a migration of monocytes expressing specific CDR3 variants to the tumor microenvironment and selection in situ. This is in accordance with a current study showing that 85% of the TAM population in glioma are comprised of infiltrating monocytes and macrophages . It might be conceivable that even more patients show shared CDR3 variants between the blood and tumor compartment with a more sensitive NGS-based repertoire analysis method. To analyze this aspect in more detail, a study using RACE-PCR and NGS for glioblastoma patients in comparison to healthy controls is currently undertaken in our laboratories. Furthermore, the shared immunoglobulin variants represent interesting target molecules and will be investigated in the future.
So far, the phenotype of the CD14+ immunoglobulin expressing macrophages (M1 or M2 category) is ambiguous and further analyses including single-cell transcriptomics in combination with immune receptor profiling are urgently needed to characterize this specific subpopulation in more detail. Moreover, investigation of the antigen specificity of the myeloid immunoglobulins will help to further uncover the role of tumor-associated macrophages in glioblastoma. Since TAM are discussed as potential targets in glioblastoma therapy , immunoglobulins expressed by TAM might have an impact on future therapeutic approaches.
In conclusion, the expression of variable immunoglobulins in monocytes and TAM can be a useful tool for the characterization of the tumor-infiltrating myeloid cells, as a therapeutic target or as a diagnostic marker for glioblastoma patients.
chemokine (C–C motif) ligand 2, also referred to as monocyte chemoattractant protein 1 (MCP1)
chemokine (C–C motif) ligand 22, also referred to as macrophage-derived chemokine (MDC)
chemokine (C–C motif) ligand 4, also referred to as macrophage Inflammatory protein 1-alpha (MIP1α)
cluster of differentiation
C-X-C motif chemokine 8, also referred to as Interleukin 8 (IL-8)
C-X-C motif chemokine 10, also referred to as Interferon gamma-induced protein 10 (IP-10)
epidermal growth factor
polymerase chain reaction
T cell receptor
tumor-necrosis factor alpha
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SBu, TF, MS-R and MN conceptualized and designed the study. SB and MT conducted the experiments. AA analyzed the tumor volume of the glioblastoma patients. SBr, AA, DH and MS-R recruited the GBM-patients and held the explanatory meetings. SBu, TF and MN analyzed and interpreted the data. SBu and TF drafted the manuscript. MN revised the manuscript for important intellectual content. All authors read and approved the final manuscript.
We thank Dr. Christian Sauer (Department of Pathology, Medical Faculty Mannheim of Heidelberg University, Germany) for sequencing analysis and Prof. David Capper (Department of Neuropathology, University Hospital Heidelberg) for the disposal of immunohistological tissue sections and stainings. We acknowledge financial support by Deutsche Forschungsgemeinschaft within the funding programme Open Access Publishing, by the Baden-Württemberg Ministry of Science, Research and the Arts and by Ruprecht-Karls-Universität Heidelberg.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Consent for publication
Written informed consent for publication of all participants in this study has been obtained.
Ethics approval and consent to participate
The use of the tumor und blood samples was approved by the Ethics Committee of the Medical Faculty Mannheim, University of Heidelberg (Permit Number: 2014-562N-MA).
The study supported by a Grant from “Stiftung für Pathobiochemie und Molekulare Diagnostik” of the “Deutschen Vereinten Gesellschaft für Klinische Chemie und Labormedizin” (FUCHS 5-2015) and the intramural funding program MEAMEDMA of the Medical Faculty Mannheim of Heidelberg University, Germany to TF (81000186).
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