Cancer research

Cancer Research: SL-28 and Leukocyte-Tells

Cancer remains one of the most difficult challenges in medicine, particularly for patients with advanced solid tumors that have progressed after surgery, chemotherapy, radiation therapy, targeted therapy, or immunotherapy. Despite decades of progress, many advanced solid tumors remain resistant to existing treatment approaches, creating an urgent need for new therapeutic strategies.

The Human Microbiology Institute’s cancer research is focused on discovering and developing new biological approaches that may help overcome the limitations of current cancer therapies. A major direction of this work is connected to the development of SL-28, also known as Leukocyte-Tells — a novel investigational cell therapy platform being advanced by Second Life Therapeutics.

Second Life Therapeutics describes SL-28 as a first-in-class, allogeneic, non-genetically modified cell therapy designed for advanced solid tumors. The company’s public materials state that SL-28 is based on donor-derived immune cells that are transformed into Leukocyte-Tells through modulation of the Universal Receptive System and its Teazeled receptors, or TezRs.

SL-28: A New Direction in Cell Therapy

SL-28 represents a new approach to anticancer cell therapy. Unlike autologous therapies that require cells to be collected from each individual patient, SL-28 is being developed as an off-the-shelf, allogeneic therapy derived from healthy donor leukocytes. This approach may allow treatment to begin without the long manufacturing delays associated with patient-specific cell therapies.

SL-28 is also non-genetically modified, distinguishing it from many existing cell therapy platforms. Instead of relying on genetic engineering against a single tumor-associated antigen, Leukocyte-Tells are designed to activate multiple anticancer mechanisms through regulation of immune cell activity and cellular memory.

The Science Behind Leukocyte-Tells

The scientific foundation of SL-28 is based on the discovery of the Universal Receptive System, a newly described regulatory system involving surface-associated nucleic acid-based receptors known as Teazeled receptors, or TezRs. By modulating these receptors, researchers generated Leukocyte-Tells with enhanced immune-cell functions.

Published research reports that Leukocyte-Tells demonstrated increased activity in pathways related to immune cell signaling, migration, endocytosis, phagocytosis, and energy metabolism. In vitro studies also showed enhanced antimicrobial and anticancer activity compared with control leukocytes.

This research suggests that Leukocyte-Tells may represent a new class of immune cells whose anticancer properties are not limited to a single tumor antigen or cancer type.

Focus on Advanced Solid Tumors

Advanced solid tumors are often diagnosed late, may spread to distant organs, and frequently become resistant to available therapies. Second Life Therapeutics is currently developing SL-28 for a broad range of advanced solid tumors, including tumor types in head and neck, thoracic, gastrointestinal, genitourinary, gynecologic, breast, and skin cancers.

The company is conducting a Phase 1/2a clinical trial evaluating the safety, pharmacokinetics, and anti-tumor activity of SL-28 as a monotherapy in patients with advanced solid tumors, including patients who have failed prior chemotherapy or immunotherapy.

Clinical and Translational Research

Early clinical observations under expanded access have provided encouraging signals in patients with advanced solid tumors. For example, a published case report described a partial response in a patient with metastatic pancreatic cancer treated with SL-28, including reductions in liver and bone metastases, with no serious adverse effects reported in that case.

These early observations require further evaluation in controlled clinical studies. SL-28 remains an investigational therapy, and its safety and effectiveness have not yet been fully established or approved by regulatory authorities.

HMI’s Research Direction

HMI’s cancer research is dedicated to understanding the biological mechanisms that regulate immune cell activity, cellular memory, tumor recognition, and resistance to therapy. Through this work, HMI aims to contribute to the development of novel therapeutic strategies for patients with advanced cancers, especially those with limited treatment options.

The institute’s research interests include:

  • Universal Receptive System biology — Studying how TezRs and related mechanisms regulate cellular memory, immune-cell activity, and interactions between host cells, microorganisms, and cancer cells.
  • Leukocyte-Tells and immune-cell modulation — Investigating how donor-derived leukocytes can be transformed into highly active immune cells with enhanced anticancer functions.
  • Advanced solid tumors — Exploring new therapeutic approaches for treatment-resistant solid tumors, including pancreatic, prostate, lung, colorectal, liver, ovarian, breast, melanoma, head and neck, and other cancers.
  • Cancer resistance and tumor microenvironment — Studying mechanisms that allow tumors to evade immune responses and resist conventional and advanced therapies.
  • Translational development — Supporting the movement of basic scientific discoveries into clinical-stage therapeutic programs.
Commitment to Collaboration

The Human Microbiology Institute is committed to advancing cancer research through collaboration with scientific, clinical, and biotechnology partners. HMI’s goal is to help translate discoveries in microbiology, immunology, and cellular regulation into new therapeutic approaches for patients with difficult-to-treat cancers.

Disclaimer: SL-28 / Leukocyte-Tells is an investigational therapy. It has not been approved by any regulatory authority, and its safety and effectiveness have not yet been fully established

Publications:
  1. Regulating white blood cell activity through the novel universal receptive system
    Scientific Reports (2025)
  2. The Universal Receptive System acts as a novel regulator in the production of antimicrobial and anticancer bioactive compounds by white blood cells
    Journal of Leukocyte Biology (2025)
  3. Dramatic Clinical Response to a Novel Form of Cell Therapy SL-28 in a Patient With Advanced Prostate Cancer: A Case Report
    ImmunoTargets and Therapy (2025)
  4. Partial response in a patient with skeletal and hepatic metastases following resected pancreatic cancer to the novel cell therapy SL-28: a case report
    Frontiers in Oncology (2025)
  5. Genomic characterization and assessment of the virulence and antibiotic resistance of the novel species Paenibacillus sp. strain VT-400, a potentially pathogenic bacterium in the oral cavity of patients with hematological malignancies
    Gut pathogens (2016)
  6. Complete Genome Sequence of Paenibacillus sp. Strain VT-400, Isolated from the Saliva of a Child with Acute Lymphoblastic Leukemia.
    Genome announcements (2015)
  7. Complete Genome Sequence of Paenibacillus sp. Strain VT-400, Isolated from the Saliva of a Child with Acute Lymphoblastic Leukemia.
    Genome announcements (2015)
  8. Complete Genome Sequence of Bacilli bacterium Strain VT-13-104 Isolated from the Intestine of a Patient with Duodenal Cancer.
    Genome announcements (2015)
  9. Complete Genome Sequence of the Streptococcus sp. Strain VT 162, Isolated from the Saliva of Pediatric Oncohematology Patients.
    Genome announcements (2014)

 

Complete Genome Sequence of Paenibacillus sp. strain VT-400, Isolated from the Saliva of a Child with Acute Lymphoblastic Leukemia

Genome announcements (2015)

Complete Genome Sequence of Paenibacillus sp. strain VT-400, Isolated from the Saliva of a Child with Acute Lymphoblastic Leukemia

Publication Type Journal Article
Authors George Tetz

Victor Tetz

Maria Vecherkovskaya

Abstract We report here the complete genome sequence of spore-forming Paenibacillus sp. strain VT 400, isolated from the saliva of a child with acute lymphoblastic leukemia. The genome consists of 6,986,122 bp, with a G+C content of 45.8%. It possesses 5,777 predicted protein-coding genes encoding multidrug resistance transporters, virulence factors, and resistance to chemotherapeutic drugs.
Year of Publication 2015
Journal Genome announcements
DOI 10.1128/genomeA.00894-15

Genomic characterization and assessment of the virulence and antibiotic resistance of the novel species Paenibacillus sp. strain VT-400, a potentially pathogenic bacterium in the oral cavity of patients with hematological malignancies

Publication Type Journal Article
Authors George Tetz

Victor Tetz

Maria Vecherkovskaya

Abstract Background

Paenibacillus sp. strain VT-400, a novel spore-forming bacterium, was isolated from patients with hematological malignancies.

Methods

Paenibacillus sp. strain VT-400 was isolated from the saliva of four children with acute lymphoblastic leukemia. The genome was annotated using RAST and the NCBI Prokaryotic Genome Annotation Pipeline to characterize features of antibiotic resistance and virulence factors. Susceptibility to antibiotics was determined by the Kirby–Bauer disc diffusion method. We used a mouse model of pneumonia to study virulence in vivo. Mice were challenged with 7.5 log10–9.5 log10 CFU, and survival was monitored over 7 days. Bacterial load was measured in the lungs and spleen of surviving mice 48 h post-infection to reveal bacterial invasion and dissemination.

Results

Whole-genome sequencing revealed a large number of virulence factors such as hemolysin D and CD4+ T cell-stimulating antigen. Furthermore, the strain harbors numerous antibiotic resistance genes, including small multidrug resistance proteins, which have never been previously found in the Paenibacillus genus. We then compared the presence of antibiotic resistance genes against results from antibiotic susceptibility testing. Paenibacillus sp. strain VT-400 was found to be resistant to macrolides such as erythromycin and azithromycin, as well as to chloramphenicol and trimethoprim–sulphamethoxazole. Finally, the isolate caused mortality in mice infected with ≥8.5 log10 CFU.

Conclusions

Based on our results and on the available literature, there is yet no strong evidence that shows Paenibacillus species as an opportunistic pathogen in immunocompromised patients. However, the presence of spore-forming bacteria with virulence and antibiotic resistance genes in such patients warrants special attention because infections caused by spore-forming bacteria are poorly treatable.

Year of Publication 2016
Journal Gut Pathogens
DOI 10.1186/s13099-016-0089-1

Complete Genome Sequence of the Streptococcus sp. strain VT-162, Isolated from the Saliva of Pediatric Oncohematology Patients

Publication Type Journal Article
Authors George Tetz

Maria F. Vecherkovskaya

Victor Tetz

Abstract Streptococcus sp. strain VT 162 was isolated from the saliva of pediatric oncohematology patients. Its full genome is 2,045,418 bp. The availability of this genome will provide insights into the composition of microbial flora among pediatric oncohematology patients and the host interaction and pathogenicity of this species.
Year of Publication 2014
Journal Genome announcements
DOI 10.1128/genomeA.00647-14

Complete genome sequence of Bacilli bacterium strain VT-13-104 isolated from the intestine of a patient with duodenal cancer.

Publication Type Journal Article
Authors George Tetz

Victor Tetz

Abstract We report the complete genome sequence of Bacilli bacterium strain VT-13-104 isolated from the intestine of a patient with duodenal cancer. The genome is composed of 3,573,421 bp, with a G+C content of 35.7%. It possesses 3,254 predicted protein-coding genes encoding multidrug resistance transporters, resistance to antibiotics, and virulence factors.
Year of Publication 2015
Journal Genome announcements
DOI 10.1128/genomeA.00705-15

Draft Genome Sequence of Acinetobacter sp. strain VT-511 Isolated from the Stomach of a Patient with Gastric Cancer

Publication Type Journal Article
Authors George Tetz

Victor Tetz

Abstract We report the draft genome sequence of Acinetobacter sp. strain VT-511, which was obtained from the stomach of a patient with gastric cancer. The genome of Acinetobacter sp. VT-511 is composed of approximately 3,416,321 bp and includes 3,214 predicted protein-coding genes.
Year of Publication 2015
Journal Genome announcements
DOI 10.1128/genomeA.01202-15