Immunogenicity Risk

A protein therapeutic can provoke antibodies against itself, and when it does the drug stops working — or worse, cross-reacts with an endogenous counterpart. This skill locates the sequence regions responsible and puts them in proportion against the factors that usually matter more.

No installation, no network, no key for the bundled scripts. Running the predictor needs NetMHCIIpan from DTU Health Tech, free for academic use under a signed licence and not redistributable — which is why these scripts prepare its input and parse its output rather than wrapping it.

Read references/running-netmhciipan.md before your first scan, references/deimmunisation.md before changing a sequence, and references/what-drives-ada.md before drawing a conclusion — that one is judgement, not syntax, and it is mostly about what the scan cannot see.

The two scripts

Class II, and %Rank

Two things to get right before anything else.

Anti-drug antibodies need CD4 T-cell help, which is class II restricted. Scanning a biologic against MHC-I answers a question about cytotoxic T cells that is rarely the one being asked. Use NetMHCIIpan.

Use %Rank, not affinity. Predicted IC50 is not comparable between alleles — each has its own affinity distribution — so nM cannot be thresholded uniformly. %Rank normalises against a background of random peptides and can. Conventionally ≤2% is a strong binder, ≤10% weak.

Collapse peptides to cores, then count alleles

python skills/immunogenicity/scripts/epitope_scan.py peptides --sequence-file mab.fa > peptides.txt
# netMHCIIpan -f peptides.txt -inptype 1 -a DRB1_0101,... -xls -xlsfile out.txt
python skills/immunogenicity/scripts/epitope_scan.py parse --output out.txt

core       example_peptide  alleles_bound  allele_coverage_pct  best_rank  promiscuous
LVESGGGLV  EVQLVESGGGLVQPG  3              75.0                 0.85       true

Consecutive 15-mers overlap by 14 residues and share a 9-mer core, so peptide hits overcount epitopes by up to sevenfold. Three predictions here collapse to one epitope.

Promiscuity matters more than potency. A core binding one rare allele affects few patients; one binding eight common alleles affects most of them. The scripts sort by alleles bound, not by rank.

Germline identity dominates the epitope count

python skills/immunogenicity/scripts/ada_risk.py score --cores cores.tsv --length 120 --humanness 0.92

A fully human sequence contains plenty of predicted class II binders — human proteins are full of them. What makes it low-risk is central tolerance: T cells recognising self-peptides were deleted in the thymus.

So the location of an epitope matters far more than the count. Peptides in germline framework are largely noise; peptides in CDRs, engineered junctions, and non-human segments are the signal. ada_risk.py changes its interpretation based on --humanness, and says so when you omit it.

Aggregation probably matters more than your sequence

The single largest non-sequence factor. Aggregates present repetitive epitope arrays that cross-link B-cell receptors and are taken up by antigen-presenting cells far more efficiently than monomer.

A low-epitope sequence that aggregates in the vial will be more immunogenic than a higher-epitope one that does not. Behind it: route (subcutaneous > IV), dosing frequency, patient population, concomitant immunosuppression, impurities, and non-human glycans — which are epitopes in their own right and invisible to any sequence scan.

Nothing here predicts an ADA rate

python skills/immunogenicity/scripts/ada_risk.py context

Humanisation helps and does not decide it — fully human adalimumab reaches 26%. Clinical ADA spans under 1% to over 60%, and no in-silico method resolves that range. Anything claiming to predict a percentage is overselling.

Deimmunising without breaking the molecule

The highest-leverage change is usually a substitution at P1 of the 9-mer core, replacing a large hydrophobic with something charged or small polar. But a substitution that breaks one core routinely creates a new one shifted a few residues along — the class II groove is open-ended, so suppressing the best register promotes the next.

Re-scan the whole molecule after every change, not just the mutated peptide. And rescreen for what you may have introduced: N-X-S/T sequons (glycoengineering), NG or DG hotspots (antibody-engineering), and aggregation propensity.

Composing with the rest of the bundle

• antibody-engineering → before: germline identity, CDR boundaries, and Vernier residues, which is the context every epitope needs.
• glycoengineering → alongside: non-human glycans are immunogenic epitopes no sequence scan finds, and deimmunising substitutions can create new sequons.
• protein-binder-design → here: de novo binders are entirely non-germline, so this scan is not optional for them.
• esm → alongside: sequence likelihood as a rough humanness proxy when no germline reference fits.
• adaptyv → after: get the variants made and tested.

Reporting results honestly

Say where the promiscuous epitopes are, not just how many. Give germline identity alongside. Name the alleles scanned and note that DP and DQ were not. State that aggregation and route are likely larger contributors than sequence. Call the output a triage aid, and recommend MAPPs or a T-cell proliferation assay before any decision that matters. Never report a predicted ADA rate.