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Multi-modal contrastive learning adapts to intrinsic dimensions of shared latent variables

NeurIPS 2025 · Label-efficient and robust learning › Self-supervised and contrastive · approach: Inductive bias and minimal representations · 0 citations (OpenAlex)

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Theoretical analysis of multi-modal contrastive (CLIP-style infoNCE) learning with temperature optimization, showing minimizers are sufficient, similarity-maximizing, and adapt to the intrinsic dimension of shared latent variables, validated on synthetic and CITE-seq data.

Problem

Existing theory of CLIP-style multi-modal contrastive learning assumes linear representations, factor-model data, or a fixed/ignored temperature, and cannot explain why learned representations adapt to a lower intrinsic dimension than the user-specified output dimension.

Approach

Using a discretized, fine-grained mutual-information order and a variational decomposition of the infoNCE loss with optimized temperature, the paper shows that infoNCE minimizers over general measurable function classes are aligned, sufficient, have constant positive-pair similarity, temperature tending to zero, and intrinsic dimension equal to the shared-latent dimension k*, without requiring uni

Key results

Measured effects reported in the paper

What was changedWhereMeasuredEffect
increase output dimension beyond 5multi-modal contrastive learning with 5-layer ReLU encoders · Synthetic data, linear and nonlinear settingstop-1 matching accuracyNo clear effect
increase output dimension beyond 5multi-modal contrastive learning with 5-layer ReLU encoders · Synthetic data, linear and nonlinear settingsestimated intrinsic dimension: k^* = 5No clear effect
train with optimized temperaturemulti-modal contrastive learning · Synthetic data, linear and nonlinear settingstemperatureHelped
increase output dimension beyond 10multi-modal contrastive learning with 5-layer ReLU encoders · CITE-seq healthy human bone marrow cellsmatching accuracyNo clear effect
increase output dimension beyond 10multi-modal contrastive learning with 5-layer ReLU encoders · CITE-seq healthy human bone marrow cellsestimated intrinsic dimension: 10No clear effect
learn representations with multi-modal contrastive loss5-layer ReLU encoders · CITE-seq healthy human bone marrow cellscell-type classification accuracyHelped

Surprising findings

Limitations

Experimental setup

Datasets: synthetic Gaussian linear and nonlinear data CITE-seq healthy human bone marrow cells (via Seurat) ImageNetV2 (appendix) YFCC (appendix)

Benchmarks: CITE-seq top-0.5% matching accuracy CITE-seq cell-type classification synthetic top-1 matching accuracy

Metrics: top-alpha% matching accuracy classification accuracy MLE intrinsic dimension estimate temperature convergence similarity histograms

Baselines: linear-representation CLIP theory alignment-uniformity analysis

Builds on: CLIP infoNCE alignment and uniformity (Wang & Isola) infoMax principle

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