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Autologous Cell Therapies for Cartilage Regeneration in the Knee

TETEC offers two matrix-associated autologous chondrocyte transplantation (MACT) procedures for the treatment of focal cartilage defects in the knee: Injectable MACT and Scaffold-Based MACT. Both use a patient's own cultured chondrocytes to support cartilage regeneration. Learn more about these treatment procedures and their role in clinical practice.

Eine Pipette träufelt eine klare Flüssigkeit auf ein biegsames transparentes Gelpolster.

Cartilage Lesions of the Knee

Cartilage defects of the knee are a common orthopedic diagnosis. As a result, several thousand surgical interventions are performed in Germany each year to treat cartilage defects of the knee. Without appropriate treatment, these defects may progress and can contribute to the development of osteoarthritis over time [1-3].

Common Causes of Cartilage Lesions of the Knee

Acute traumatic injuries, including sports-related injuries

Repetitive overuse or abnormal joint loading

Osteochondritis dissecans (OCD)

Malalignment or chronic joint instability

Why Cartilage Heals Poorly

The lack of a direct blood supply limits the availability of nutrients and reparative cells

Low cellular activity slows extracellular matrix regeneration

The dense extracellular matrix restricts cell migration

Excessive or persistent loading may impair healing and promote cartilage degeneration

TREATMENT LANDSCAPE

Established Treatment Procedures Compared

For the treatment of cartilage defects of the knee, several procedures are available, including bone marrow stimulation (BMS), matrix-augmented BMS, osteochondral autograft transfer (OAT), and matrix-associated autologous chondrocyte transplantation (MACT). The choice of treatment depends on several factors, including defect size.

UP TO 1.5 cm2

Osteochondral
Transplantation

UP TO 2 cm2

Bone Marrow Stimulation

1-4.5 cm2

Matrix-Augmented Bone Marrow Stimulation

2-10 cm2

Scaffold-based MACT (Matrix-Associated Autologous Chondrocyte Transplantation)

≥ 2 cm2

Injectable MACT (Matrix-Associated Autologous Chondrocyte Transplantation)

0 cm2

1 cm2

2 cm2

3 cm2

4 cm2

5 cm2

6 cm2

7 cm2

8 cm2

9 cm2

10 cm2

11 cm2

The graphic is based on recommendations from the DGOU Clinical Tissue Regeneration Working Group for the treatment of cartilage defects of the knee and on defect-size information provided in the respective Summary of Product Characteristics (SmPCs) [4-6]. In addition to defect size, the selection of the most appropriate treatment should always take into account the patient's individual clinical situation.
TETEC PROCEDURES COMPARED

Injectable MACT vs. Scaffold-Based MACT

Explore Injectable MACT and Scaffold-Based MACT in greater detail.

Injectable MACT
Scaffold-Based MACT
Surgical Approach
Arthroscopic [7]
Mini-arthrotomy [8]
Method of Fixation
None (in situ cross-linking hydrogel ≤3 min) [7]
Sutures [5]
Handling
No trimming required
Scaffold trimmed to defect size
Procedure Time
15–40 minutes [7, 9]
~60 minutes [10]
Defect Size
≥ 2 cm² [6]
2–10 cm² [5]
TETEC Products

Cell-Based Cartilage Regeneration for the Knee

TETEC offers two products for the treatment of knee cartilage defects within the framework of autologous chondrocyte transplantation: an injectable, hydrogel-based cartilage cell transplant (Injectable MACT) and a cartilage cell transplant with a collagen scaffold (Scaffold-Based MACT).

Ein Arzt hält ein anatomisches Modell eines Knies und zeigt darauf mit einem Stift.
Injectable MACT

Injectable MACT is a cell-based procedure for the treatment of focal cartilage defects of the knee. The procedure uses a patient's own cartilage cells in combination with an injectable hydrogel for transplantation into the cartilage defect [6]. In clinical studies and earlier publications, this procedure has also been referred to as hydrogel-based ACI or Injectable M-ACI.

  • A patient's own cartilage cells suspended in an injectable hydrogel
  • Minimally invasive arthroscopic transplantation
About Injectable MACT
Illustration eines Knies mit hervorgehobener Kniescheibe und Bändern.
Scaffold-Based MACT

In Scaffold-Based MACT, a patient's own cartilage cells are seeded onto a collagen-based scaffold and transplanted into the cartilage defect [5].

  • Collagen-based scaffold seeded with a patient's own cartilage cells
  • Transplantation via a small surgical approach (mini-arthrotomy)
About Scaffold-based MACT

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Literature

1. Ding C, Cicuttini F, Scott F, Boon C, Jones G. Association of prevalent and incident knee cartilage defects with loss of tibial and patellar cartilage: a longitudinal study. Arthritis Rheum. 2005;52(12):3918–3927.

2. Cicuttini F, Ding C, Wluka A, Davis S, Ebeling PR, Jones G. Association of cartilage defects with loss of knee cartilage in healthy, middle-aged adults: a prospective study. Arthritis Rheum. 2005;52(7):2033–2039.

3. Houck DA, Kraeutler MJ, Belk JW, Frank RM, McCarty EC, Bravman JT. Do focal chondral defects of the knee increase the risk for progression to osteoarthritis? Orthop J Sports Med. 2018;6(10):2325967118801931.

4. Niemeyer P, Albrecht D, Aurich M, et al. Empfehlungen der AG Klinische Geweberegeneration zur Behandlung von Knorpelschäden am Kniegelenk. Z Orthop Unfall. 2023;161(1):57–64.

5. TETEC AG. Summary of Product Characteristics (SmPC) NOVOCART® 3D. Reutlingen (DE): TETEC AG; 2023. Revision date: 11/2023. PEI.A.11511.01.1.

6. TETEC AG. Summary of Product Characteristics (SmPC) NOVOCART® Inject. Reutlingen (DE): TETEC AG; 2026. Revision date: 02/2026. PEI.A.11763.01.1.

7. Niemeyer P, Hanus M, Belickas J, et al. Treatment of large cartilage defects in the knee by hydrogel-based autologous chondrocyte implantation: two-year results of a prospective, multicenter, single-arm phase III trial. Cartilage. 2022;13(1):19476035221085146.

8. Paul-Ehrlich-Institut. Physician training guide for NOVOCART 3D. Langen (DE): PEI; 2025.

9. Schlumberger M, Schuster P, Bülow HJ, et al. Arthroscopic autologous chondrocyte implantation in the knee with an in situ crosslinking matrix: minimum 4-year clinical results of 15 cases and 1 histological evaluation. Arch Orthop Trauma Surg. 2019;139(11):1607–1615.

10. Data on file. Study report NOVOCART 3D Phase III (AAG-G-H-1202)